Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

Care4Rare Canada Consortium; Undiagnosed Diseases Network; Sureni V. Mullegama; Kaitlyn A. Kiernan; Erin Torti; Ethan Pavlovsky; Nicholas Tilton; Austin Sekula; Hua Gao; Joseph T. Alaimo; Kendra Engleman; Eric T. Rush; Karli Blocker; Katrina M. Dipple; Veronica M. Fettig; Heather Hare; Ian Glass; Dorothy K. Grange; Michael Griffin; Chanika Phornphutkul; Lauren Massingham; Lakshmi Mehta; Danny E. Miller; Jenny Thies; J. Lawrence Merritt; Eric Muller; Matthew Osmond; Sarah L. Sawyer; Rachel Slaugh; Rachel E. Hickey; Barry Wolf; Sanjeev Choudhary; Miljan Simonović; Yueqing Zhang; Timothy Blake Palculict; Aida Telegrafi; Deanna Alexis Carere; Ingrid M. Wentzensen; Michelle M. Morrow; Kristin G. Monaghan; Jane Juusola; Jun Yang

doi:10.1016/j.ajhg.2024.05.004

Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

Care4Rare Canada Consortium, Undiagnosed Diseases Network, Sureni V. Mullegama, Kaitlyn A. Kiernan, Erin Torti, Ethan Pavlovsky, Nicholas Tilton, Austin Sekula, Hua Gao, Joseph T. Alaimo, Kendra Engleman, Eric T. Rush, Karli Blocker, Katrina M. Dipple, Veronica M. Fettig, Heather Hare, Ian Glass, Dorothy K. Grange, Michael Griffin, Chanika PhornphutkulLauren Massingham, Lakshmi Mehta, Danny E. Miller, Jenny Thies, J. Lawrence Merritt, Eric Muller, Matthew Osmond, Sarah L. Sawyer, Rachel Slaugh, Rachel E. Hickey, Barry Wolf, Sanjeev Choudhary, Miljan Simonović, Yueqing Zhang, Timothy Blake Palculict, Aida Telegrafi, Deanna Alexis Carere, Ingrid M. Wentzensen, Michelle M. Morrow, Kristin G. Monaghan, Jane Juusola, Jun Yang

Research output: Contribution to journal › Comment/debate

Abstract

(The American Journal of Human Genetics 111, 778–790; April 4, 2024) In the originally published version of the paper, the placement of the final two authors was incorrect. Both Jane Juusola and Jun Yang are co-senior authors; J.J. should appear second-to-last and J.Y. appear last. The authors apologize for this error.

Original language	English
Pages (from-to)	1240
Number of pages	1
Journal	American journal of human genetics
Volume	111
Issue number	6
DOIs	https://doi.org/10.1016/j.ajhg.2024.05.004
State	Published - Jun 6 2024

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Care4Rare Canada Consortium, Undiagnosed Diseases Network, Mullegama, S. V., Kiernan, K. A., Torti, E., Pavlovsky, E., Tilton, N., Sekula, A., Gao, H., Alaimo, J. T., Engleman, K., Rush, E. T., Blocker, K., Dipple, K. M., Fettig, V. M., Hare, H., Glass, I., Grange, D. K., Griffin, M., ... Yang, J. (2024). Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016)). American journal of human genetics, 111(6), 1240. https://doi.org/10.1016/j.ajhg.2024.05.004

Care4Rare Canada Consortium ; Undiagnosed Diseases Network ; Mullegama, Sureni V. et al. / Erratum : De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016)). In: American journal of human genetics. 2024 ; Vol. 111, No. 6. pp. 1240.

@article{89502dec67be4ab8ae5d78b494559bf0,

title = "Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))",

abstract = "(The American Journal of Human Genetics 111, 778–790; April 4, 2024) In the originally published version of the paper, the placement of the final two authors was incorrect. Both Jane Juusola and Jun Yang are co-senior authors; J.J. should appear second-to-last and J.Y. appear last. The authors apologize for this error.",

author = "{Care4Rare Canada Consortium} and {Undiagnosed Diseases Network} and Mullegama, {Sureni V.} and Kiernan, {Kaitlyn A.} and Erin Torti and Ethan Pavlovsky and Nicholas Tilton and Austin Sekula and Hua Gao and Alaimo, {Joseph T.} and Kendra Engleman and Rush, {Eric T.} and Karli Blocker and Dipple, {Katrina M.} and Fettig, {Veronica M.} and Heather Hare and Ian Glass and Grange, {Dorothy K.} and Michael Griffin and Chanika Phornphutkul and Lauren Massingham and Lakshmi Mehta and Miller, {Danny E.} and Jenny Thies and Merritt, {J. Lawrence} and Eric Muller and Matthew Osmond and Sawyer, {Sarah L.} and Rachel Slaugh and Hickey, {Rachel E.} and Barry Wolf and Sanjeev Choudhary and Miljan Simonovi{\'c} and Yueqing Zhang and Palculict, {Timothy Blake} and Aida Telegrafi and Carere, {Deanna Alexis} and Wentzensen, {Ingrid M.} and Morrow, {Michelle M.} and Monaghan, {Kristin G.} and Jane Juusola and Jun Yang",

note = "Publisher Copyright: {\textcopyright} 2024 American Society of Human Genetics",

year = "2024",

month = jun,

day = "6",

doi = "10.1016/j.ajhg.2024.05.004",

language = "English",

volume = "111",

pages = "1240",

journal = "American journal of human genetics",

issn = "0002-9297",

number = "6",

}

Care4Rare Canada Consortium, Undiagnosed Diseases Network, Mullegama, SV, Kiernan, KA, Torti, E, Pavlovsky, E, Tilton, N, Sekula, A, Gao, H, Alaimo, JT, Engleman, K, Rush, ET, Blocker, K, Dipple, KM, Fettig, VM, Hare, H, Glass, I, Grange, DK, Griffin, M, Phornphutkul, C, Massingham, L, Mehta, L, Miller, DE, Thies, J, Merritt, JL, Muller, E, Osmond, M, Sawyer, SL, Slaugh, R, Hickey, RE, Wolf, B, Choudhary, S, Simonović, M, Zhang, Y, Palculict, TB, Telegrafi, A, Carere, DA, Wentzensen, IM, Morrow, MM, Monaghan, KG, Juusola, J & Yang, J 2024, 'Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))', American journal of human genetics, vol. 111, no. 6, pp. 1240. https://doi.org/10.1016/j.ajhg.2024.05.004

Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016)). / Care4Rare Canada Consortium; Undiagnosed Diseases Network; Mullegama, Sureni V. et al.
In: American journal of human genetics, Vol. 111, No. 6, 06.06.2024, p. 1240.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

AU - Care4Rare Canada Consortium

AU - Undiagnosed Diseases Network

AU - Mullegama, Sureni V.

AU - Kiernan, Kaitlyn A.

AU - Torti, Erin

AU - Pavlovsky, Ethan

AU - Tilton, Nicholas

AU - Sekula, Austin

AU - Gao, Hua

AU - Alaimo, Joseph T.

AU - Engleman, Kendra

AU - Rush, Eric T.

AU - Blocker, Karli

AU - Dipple, Katrina M.

AU - Fettig, Veronica M.

AU - Hare, Heather

AU - Glass, Ian

AU - Grange, Dorothy K.

AU - Griffin, Michael

AU - Phornphutkul, Chanika

AU - Massingham, Lauren

AU - Mehta, Lakshmi

AU - Miller, Danny E.

AU - Thies, Jenny

AU - Merritt, J. Lawrence

AU - Muller, Eric

AU - Osmond, Matthew

AU - Sawyer, Sarah L.

AU - Slaugh, Rachel

AU - Hickey, Rachel E.

AU - Wolf, Barry

AU - Choudhary, Sanjeev

AU - Simonović, Miljan

AU - Zhang, Yueqing

AU - Palculict, Timothy Blake

AU - Telegrafi, Aida

AU - Carere, Deanna Alexis

AU - Wentzensen, Ingrid M.

AU - Morrow, Michelle M.

AU - Monaghan, Kristin G.

AU - Juusola, Jane

AU - Yang, Jun

PY - 2024/6/6

Y1 - 2024/6/6

N2 - (The American Journal of Human Genetics 111, 778–790; April 4, 2024) In the originally published version of the paper, the placement of the final two authors was incorrect. Both Jane Juusola and Jun Yang are co-senior authors; J.J. should appear second-to-last and J.Y. appear last. The authors apologize for this error.

AB - (The American Journal of Human Genetics 111, 778–790; April 4, 2024) In the originally published version of the paper, the placement of the final two authors was incorrect. Both Jane Juusola and Jun Yang are co-senior authors; J.J. should appear second-to-last and J.Y. appear last. The authors apologize for this error.

UR - http://www.scopus.com/inward/record.url?scp=85192948793&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2024.05.004

DO - 10.1016/j.ajhg.2024.05.004

M3 - Comment/debate

C2 - 38749428

AN - SCOPUS:85192948793

SN - 0002-9297

VL - 111

SP - 1240

JO - American journal of human genetics

JF - American journal of human genetics

IS - 6

ER -

Care4Rare Canada Consortium, Undiagnosed Diseases Network, Mullegama SV, Kiernan KA, Torti E, Pavlovsky E et al. Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016)). American journal of human genetics. 2024 Jun 6;111(6):1240. doi: 10.1016/j.ajhg.2024.05.004

Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

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