Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013))

Elizabeth E. Palmer; Seungbeom Hong; Fatema Al Zahrani; Mais O. Hashem; Fajr A. Aleisa; Heba M. Jalal Ahmed; Tejaswi Kandula; Rebecca Macintosh; Andre E. Minoche; Clare Puttick; Velimir Gayevskiy; Alexander P. Drew; Mark J. Cowley; Marcel Dinger; Jill A. Rosenfeld; Rui Xiao; Megan T. Cho; Suliat F. Yakubu; Lindsay B. Henderson; Maria J. Guillen Sacoto; Amber Begtrup; Muddathir Hamad; Marwan Shinawi; Marisa V. Andrews; Marilyn C. Jones; Kristin Lindstrom; Ruth E. Bristol; Saima Kayani; Molly Snyder; Marıá Mercedes Villanueva; Angeles Schteinschnaider; Laurence Faivre; Christel Thauvin; Antonio Vitobello; Tony Roscioli; Edwin P. Kirk; Ann Bye; Jasmeen Merzaban; Łukasz Jaremko; Mariusz Jaremko; Rani K. Sachdev; Fowzan S. Alkuraya; Stefan T. Arold

doi:10.1016/j.ajhg.2019.03.016

Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013))

Elizabeth E. Palmer, Seungbeom Hong, Fatema Al Zahrani, Mais O. Hashem, Fajr A. Aleisa, Heba M. Jalal Ahmed, Tejaswi Kandula, Rebecca Macintosh, Andre E. Minoche, Clare Puttick, Velimir Gayevskiy, Alexander P. Drew, Mark J. Cowley, Marcel Dinger, Jill A. Rosenfeld, Rui Xiao, Megan T. Cho, Suliat F. Yakubu, Lindsay B. Henderson, Maria J. Guillen SacotoAmber Begtrup, Muddathir Hamad, Marwan Shinawi, Marisa V. Andrews, Marilyn C. Jones, Kristin Lindstrom, Ruth E. Bristol, Saima Kayani, Molly Snyder, Marıá Mercedes Villanueva, Angeles Schteinschnaider, Laurence Faivre, Christel Thauvin, Antonio Vitobello, Tony Roscioli, Edwin P. Kirk, Ann Bye, Jasmeen Merzaban, Łukasz Jaremko, Mariusz Jaremko, Rani K. Sachdev, Fowzan S. Alkuraya, Stefan T. Arold

Research output: Contribution to journal › Comment/debate

Abstract

(The American Journal of Human Genetics 104, 542–552; March 7, 2019) In the original version of this article published on March 7, 2019, Łukasz Jaremko's name was unfortunately misspelled as Łukas Jaremko. It appears correctly here and online. The Journal and the authors apologize for this error.

Original language	English
Pages (from-to)	778
Number of pages	1
Journal	American journal of human genetics
Volume	104
Issue number	4
DOIs	https://doi.org/10.1016/j.ajhg.2019.03.016
State	Published - Apr 4 2019

Access to Document

10.1016/j.ajhg.2019.03.016

Fingerprint

Dive into the research topics of 'Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013))'. Together they form a unique fingerprint.

Cite this

Palmer, E. E., Hong, S., Al Zahrani, F., Hashem, M. O., Aleisa, F. A., Jalal Ahmed, H. M., Kandula, T., Macintosh, R., Minoche, A. E., Puttick, C., Gayevskiy, V., Drew, A. P., Cowley, M. J., Dinger, M., Rosenfeld, J. A., Xiao, R., Cho, M. T., Yakubu, S. F., Henderson, L. B., ... Arold, S. T. (2019). Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013)). American journal of human genetics, 104(4), 778. https://doi.org/10.1016/j.ajhg.2019.03.016

Palmer, Elizabeth E. ; Hong, Seungbeom ; Al Zahrani, Fatema et al. / Erratum : De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013)). In: American journal of human genetics. 2019 ; Vol. 104, No. 4. pp. 778.

@article{f722affa564a4a7f95d7938d66fe9dc5,

title = "Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013))",

abstract = "(The American Journal of Human Genetics 104, 542–552; March 7, 2019) In the original version of this article published on March 7, 2019, {\L}ukasz Jaremko's name was unfortunately misspelled as {\L}ukas Jaremko. It appears correctly here and online. The Journal and the authors apologize for this error.",

author = "Palmer, {Elizabeth E.} and Seungbeom Hong and {Al Zahrani}, Fatema and Hashem, {Mais O.} and Aleisa, {Fajr A.} and {Jalal Ahmed}, {Heba M.} and Tejaswi Kandula and Rebecca Macintosh and Minoche, {Andre E.} and Clare Puttick and Velimir Gayevskiy and Drew, {Alexander P.} and Cowley, {Mark J.} and Marcel Dinger and Rosenfeld, {Jill A.} and Rui Xiao and Cho, {Megan T.} and Yakubu, {Suliat F.} and Henderson, {Lindsay B.} and {Guillen Sacoto}, {Maria J.} and Amber Begtrup and Muddathir Hamad and Marwan Shinawi and Andrews, {Marisa V.} and Jones, {Marilyn C.} and Kristin Lindstrom and Bristol, {Ruth E.} and Saima Kayani and Molly Snyder and Villanueva, {Marı{\'a} Mercedes} and Angeles Schteinschnaider and Laurence Faivre and Christel Thauvin and Antonio Vitobello and Tony Roscioli and Kirk, {Edwin P.} and Ann Bye and Jasmeen Merzaban and {\L}ukasz Jaremko and Mariusz Jaremko and Sachdev, {Rani K.} and Alkuraya, {Fowzan S.} and Arold, {Stefan T.}",

note = "Publisher Copyright: {\textcopyright} 2019 American Society of Human Genetics",

year = "2019",

month = apr,

day = "4",

doi = "10.1016/j.ajhg.2019.03.016",

language = "English",

volume = "104",

pages = "778",

journal = "American journal of human genetics",

issn = "0002-9297",

number = "4",

}

Palmer, EE, Hong, S, Al Zahrani, F, Hashem, MO, Aleisa, FA, Jalal Ahmed, HM, Kandula, T, Macintosh, R, Minoche, AE, Puttick, C, Gayevskiy, V, Drew, AP, Cowley, MJ, Dinger, M, Rosenfeld, JA, Xiao, R, Cho, MT, Yakubu, SF, Henderson, LB, Guillen Sacoto, MJ, Begtrup, A, Hamad, M, Shinawi, M, Andrews, MV, Jones, MC, Lindstrom, K, Bristol, RE, Kayani, S, Snyder, M, Villanueva, MM, Schteinschnaider, A, Faivre, L, Thauvin, C, Vitobello, A, Roscioli, T, Kirk, EP, Bye, A, Merzaban, J, Jaremko, Ł, Jaremko, M, Sachdev, RK, Alkuraya, FS & Arold, ST 2019, 'Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013))', American journal of human genetics, vol. 104, no. 4, pp. 778. https://doi.org/10.1016/j.ajhg.2019.03.016

Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013)). / Palmer, Elizabeth E.; Hong, Seungbeom; Al Zahrani, Fatema et al.
In: American journal of human genetics, Vol. 104, No. 4, 04.04.2019, p. 778.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013))

AU - Palmer, Elizabeth E.

AU - Hong, Seungbeom

AU - Al Zahrani, Fatema

AU - Hashem, Mais O.

AU - Aleisa, Fajr A.

AU - Jalal Ahmed, Heba M.

AU - Kandula, Tejaswi

AU - Macintosh, Rebecca

AU - Minoche, Andre E.

AU - Puttick, Clare

AU - Gayevskiy, Velimir

AU - Drew, Alexander P.

AU - Cowley, Mark J.

AU - Dinger, Marcel

AU - Rosenfeld, Jill A.

AU - Xiao, Rui

AU - Cho, Megan T.

AU - Yakubu, Suliat F.

AU - Henderson, Lindsay B.

AU - Guillen Sacoto, Maria J.

AU - Begtrup, Amber

AU - Hamad, Muddathir

AU - Shinawi, Marwan

AU - Andrews, Marisa V.

AU - Jones, Marilyn C.

AU - Lindstrom, Kristin

AU - Bristol, Ruth E.

AU - Kayani, Saima

AU - Snyder, Molly

AU - Villanueva, Marıá Mercedes

AU - Schteinschnaider, Angeles

AU - Faivre, Laurence

AU - Thauvin, Christel

AU - Vitobello, Antonio

AU - Roscioli, Tony

AU - Kirk, Edwin P.

AU - Bye, Ann

AU - Merzaban, Jasmeen

AU - Jaremko, Łukasz

AU - Jaremko, Mariusz

AU - Sachdev, Rani K.

AU - Alkuraya, Fowzan S.

AU - Arold, Stefan T.

PY - 2019/4/4

Y1 - 2019/4/4

N2 - (The American Journal of Human Genetics 104, 542–552; March 7, 2019) In the original version of this article published on March 7, 2019, Łukasz Jaremko's name was unfortunately misspelled as Łukas Jaremko. It appears correctly here and online. The Journal and the authors apologize for this error.

AB - (The American Journal of Human Genetics 104, 542–552; March 7, 2019) In the original version of this article published on March 7, 2019, Łukasz Jaremko's name was unfortunately misspelled as Łukas Jaremko. It appears correctly here and online. The Journal and the authors apologize for this error.

UR - http://www.scopus.com/inward/record.url?scp=85063617481&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2019.03.016

DO - 10.1016/j.ajhg.2019.03.016

M3 - Comment/debate

C2 - 30929740

AN - SCOPUS:85063617481

SN - 0002-9297

VL - 104

SP - 778

JO - American journal of human genetics

JF - American journal of human genetics

IS - 4

ER -

Palmer EE, Hong S, Al Zahrani F, Hashem MO, Aleisa FA, Jalal Ahmed HM et al. Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013)). American journal of human genetics. 2019 Apr 4;104(4):778. doi: 10.1016/j.ajhg.2019.03.016

Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013))

Abstract

Access to Document

Other files and links

Fingerprint

Cite this