Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))

Brooke Sadler; Jackson Wilborn; Lilian Antunes; Timothy Kuensting; Andrew T. Hale; Stephen R. Gannon; Kevin McCall; Carlos Cruchaga; Matthew Harms; Norine Voisin; Alexandre Reymond; Gerarda Cappuccio; Nicola Brunetti-Pierri; Marco Tartaglia; Marcello Niceta; Chiara Leoni; Giuseppe Zampino; Allison Ashley-Koch; Aintzane Urbizu; Melanie E. Garrett; Karen Soldano; Alfons Macaya; Donald Conrad; Jennifer Strahle; Matthew B. Dobbs; Tychele N. Turner; Chevis N. Shannon; Douglas Brockmeyer; David D. Limbrick; Christina A. Gurnett; Gabe Haller

doi:10.1016/j.ajhg.2021.01.014

Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))

Brooke Sadler, Jackson Wilborn, Lilian Antunes, Timothy Kuensting, Andrew T. Hale, Stephen R. Gannon, Kevin McCall, Carlos Cruchaga, Matthew Harms, Norine Voisin, Alexandre Reymond, Gerarda Cappuccio, Nicola Brunetti-Pierri, Marco Tartaglia, Marcello Niceta, Chiara Leoni, Giuseppe Zampino, Allison Ashley-Koch, Aintzane Urbizu, Melanie E. GarrettKaren Soldano, Alfons Macaya, Donald Conrad, Jennifer Strahle, Matthew B. Dobbs, Tychele N. Turner, Chevis N. Shannon, Douglas Brockmeyer, David D. Limbrick, Christina A. Gurnett, Gabe Haller

Research output: Contribution to journal › Comment/debate

3 Scopus citations

Abstract

(The American Journal of Human Genetics 108, 100–114; January 7, 2021) Three variants were misnamed in the text and mislabeled in Figure 2. The relevant sentence has been changed to read, “The three de novo CHD8 mutations observed in CM1 include two stop-gain mutations (GenBank: NM_001170629.2; c.4414C>T [p.Arg1472^∗] and c.4514G>A [p.Trp1505^∗]) and a splice donor site mutation (c.2907+1G>T [p.?]).” These errors have been corrected online. The authors apologize for these errors.

Original language	English
Pages (from-to)	530-531
Number of pages	2
Journal	American journal of human genetics
Volume	108
Issue number	3
DOIs	https://doi.org/10.1016/j.ajhg.2021.01.014
State	Published - Mar 4 2021

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Sadler, B., Wilborn, J., Antunes, L., Kuensting, T., Hale, A. T., Gannon, S. R., McCall, K., Cruchaga, C., Harms, M., Voisin, N., Reymond, A., Cappuccio, G., Brunetti-Pierri, N., Tartaglia, M., Niceta, M., Leoni, C., Zampino, G., Ashley-Koch, A., Urbizu, A., ... Haller, G. (2021). Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001)). American journal of human genetics, 108(3), 530-531. https://doi.org/10.1016/j.ajhg.2021.01.014

@article{ba47eb09bb554ece96e8ab67c0a8af4e,

title = "Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))",

abstract = "(The American Journal of Human Genetics 108, 100–114; January 7, 2021) Three variants were misnamed in the text and mislabeled in Figure 2. The relevant sentence has been changed to read, “The three de novo CHD8 mutations observed in CM1 include two stop-gain mutations (GenBank: NM_001170629.2; c.4414C>T [p.Arg1472∗] and c.4514G>A [p.Trp1505∗]) and a splice donor site mutation (c.2907+1G>T [p.?]).” These errors have been corrected online. The authors apologize for these errors.",

author = "Brooke Sadler and Jackson Wilborn and Lilian Antunes and Timothy Kuensting and Hale, {Andrew T.} and Gannon, {Stephen R.} and Kevin McCall and Carlos Cruchaga and Matthew Harms and Norine Voisin and Alexandre Reymond and Gerarda Cappuccio and Nicola Brunetti-Pierri and Marco Tartaglia and Marcello Niceta and Chiara Leoni and Giuseppe Zampino and Allison Ashley-Koch and Aintzane Urbizu and Garrett, {Melanie E.} and Karen Soldano and Alfons Macaya and Donald Conrad and Jennifer Strahle and Dobbs, {Matthew B.} and Turner, {Tychele N.} and Shannon, {Chevis N.} and Douglas Brockmeyer and Limbrick, {David D.} and Gurnett, {Christina A.} and Gabe Haller",

note = "Publisher Copyright: {\textcopyright} 2021 American Society of Human Genetics",

year = "2021",

month = mar,

day = "4",

doi = "10.1016/j.ajhg.2021.01.014",

language = "English",

volume = "108",

pages = "530--531",

journal = "American journal of human genetics",

issn = "0002-9297",

number = "3",

}

Sadler, B, Wilborn, J, Antunes, L, Kuensting, T, Hale, AT, Gannon, SR, McCall, K, Cruchaga, C, Harms, M, Voisin, N, Reymond, A, Cappuccio, G, Brunetti-Pierri, N, Tartaglia, M, Niceta, M, Leoni, C, Zampino, G, Ashley-Koch, A, Urbizu, A, Garrett, ME, Soldano, K, Macaya, A, Conrad, D, Strahle, J, Dobbs, MB, Turner, TN, Shannon, CN, Brockmeyer, D, Limbrick, DD, Gurnett, CA & Haller, G 2021, 'Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))', American journal of human genetics, vol. 108, no. 3, pp. 530-531. https://doi.org/10.1016/j.ajhg.2021.01.014

Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001)). / Sadler, Brooke; Wilborn, Jackson; Antunes, Lilian et al.
In: American journal of human genetics, Vol. 108, No. 3, 04.03.2021, p. 530-531.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))

AU - Sadler, Brooke

AU - Wilborn, Jackson

AU - Antunes, Lilian

AU - Kuensting, Timothy

AU - Hale, Andrew T.

AU - Gannon, Stephen R.

AU - McCall, Kevin

AU - Cruchaga, Carlos

AU - Harms, Matthew

AU - Voisin, Norine

AU - Reymond, Alexandre

AU - Cappuccio, Gerarda

AU - Brunetti-Pierri, Nicola

AU - Tartaglia, Marco

AU - Niceta, Marcello

AU - Leoni, Chiara

AU - Zampino, Giuseppe

AU - Ashley-Koch, Allison

AU - Urbizu, Aintzane

AU - Garrett, Melanie E.

AU - Soldano, Karen

AU - Macaya, Alfons

AU - Conrad, Donald

AU - Strahle, Jennifer

AU - Dobbs, Matthew B.

AU - Turner, Tychele N.

AU - Shannon, Chevis N.

AU - Brockmeyer, Douglas

AU - Limbrick, David D.

AU - Gurnett, Christina A.

AU - Haller, Gabe

PY - 2021/3/4

Y1 - 2021/3/4

N2 - (The American Journal of Human Genetics 108, 100–114; January 7, 2021) Three variants were misnamed in the text and mislabeled in Figure 2. The relevant sentence has been changed to read, “The three de novo CHD8 mutations observed in CM1 include two stop-gain mutations (GenBank: NM_001170629.2; c.4414C>T [p.Arg1472∗] and c.4514G>A [p.Trp1505∗]) and a splice donor site mutation (c.2907+1G>T [p.?]).” These errors have been corrected online. The authors apologize for these errors.

AB - (The American Journal of Human Genetics 108, 100–114; January 7, 2021) Three variants were misnamed in the text and mislabeled in Figure 2. The relevant sentence has been changed to read, “The three de novo CHD8 mutations observed in CM1 include two stop-gain mutations (GenBank: NM_001170629.2; c.4414C>T [p.Arg1472∗] and c.4514G>A [p.Trp1505∗]) and a splice donor site mutation (c.2907+1G>T [p.?]).” These errors have been corrected online. The authors apologize for these errors.

UR - http://www.scopus.com/inward/record.url?scp=85101819097&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2021.01.014

DO - 10.1016/j.ajhg.2021.01.014

M3 - Comment/debate

C2 - 33667397

AN - SCOPUS:85101819097

SN - 0002-9297

VL - 108

SP - 530

EP - 531

JO - American journal of human genetics

JF - American journal of human genetics

IS - 3

ER -

Sadler B, Wilborn J, Antunes L, Kuensting T, Hale AT, Gannon SR et al. Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001)). American journal of human genetics. 2021 Mar 4;108(3):530-531. doi: 10.1016/j.ajhg.2021.01.014

Erratum: Rare and de novo coding variants in chromodomain genes in Chiari I malformation (The American Journal of Human Genetics (2021) 108(1) (100–114), (S0002929720304377), (10.1016/j.ajhg.2020.12.001))

Abstract

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