Correction: KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants

Deciphering Developmental Disorders (DDD) Study; Joanna Kennedy; David Goudie; Edward Blair; Kate Chandler; Shelagh Joss; Victoria McKay; Andrew Green; Ruth Armstrong; Melissa Lees; Benjamin Kamien; Bruce Hopper; Tiong Yang Tan; Patrick Yap; Zornitza Stark; Nobuhiko Okamoto; Noriko Miyake; Naomichi Matsumoto; Ellen Macnamara; Jennifer L. Murphy; Elizabeth McCormick; Hakon Hakonarson; Marni J. Falk; Dong Li; Patrick Blackburn; Eric Klee; Dusica Babovic-Vuksanovic; Susan Schelley; Louanne Hudgins; Sarina Kant; Bertrand Isidor; Benjamin Cogne; Kimberley Bradbury; Mark Williams; Chirag Patel; Helen Heussler; Celia Duff-Farrier; Phillis Lakeman; Ingrid Scurr; Usha Kini; Mariet Elting; Margot Reijnders; Janneke Schuurs-Hoeijmakers; Mohamed Wafik; Anne Blomhoff; Claudia A. L. Ruivenkamp; Esther Nibbeling; Alexander J. M. Dingemans; Emilie D. Douine; Stanley F. Nelson; Maja Hempel

doi:10.1038/s41436-020-00944-7

Correction: KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants

Deciphering Developmental Disorders (DDD) Study, Joanna Kennedy, David Goudie, Edward Blair, Kate Chandler, Shelagh Joss, Victoria McKay, Andrew Green, Ruth Armstrong, Melissa Lees, Benjamin Kamien, Bruce Hopper, Tiong Yang Tan, Patrick Yap, Zornitza Stark, Nobuhiko Okamoto, Noriko Miyake, Naomichi Matsumoto, Ellen Macnamara, Jennifer L. MurphyElizabeth McCormick, Hakon Hakonarson, Marni J. Falk, Dong Li, Patrick Blackburn, Eric Klee, Dusica Babovic-Vuksanovic, Susan Schelley, Louanne Hudgins, Sarina Kant, Bertrand Isidor, Benjamin Cogne, Kimberley Bradbury, Mark Williams, Chirag Patel, Helen Heussler, Celia Duff-Farrier, Phillis Lakeman, Ingrid Scurr, Usha Kini, Mariet Elting, Margot Reijnders, Janneke Schuurs-Hoeijmakers, Mohamed Wafik, Anne Blomhoff, Claudia A. L. Ruivenkamp, Esther Nibbeling, Alexander J. M. Dingemans, Emilie D. Douine, Stanley F. Nelson, Maja Hempel

Population Health and Genomics

Research output: Contribution to journal › Article

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Original language	English
Pages (from-to)	1920
Number of pages	1
Journal	Genetics in Medicine
Volume	22
Issue number	11
Early online date	19 Aug 2020
DOIs	https://doi.org/10.1038/s41436-020-00944-7
Publication status	Published - Nov 2020

ASJC Scopus subject areas

Genetics(clinical)

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Deciphering Developmental Disorders (DDD) Study, Kennedy, J., Goudie, D., Blair, E., Chandler, K., Joss, S., McKay, V., Green, A., Armstrong, R., Lees, M., Kamien, B., Hopper, B., Tan, T. Y., Yap, P., Stark, Z., Okamoto, N., Miyake, N., Matsumoto, N., Macnamara, E., ... Hempel, M. (2020). Correction: KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants. Genetics in Medicine, 22(11), 1920. https://doi.org/10.1038/s41436-020-00944-7

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title = "Correction: KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants",

abstract = "An amendment to this paper has been published and can be accessed via a link at the top of the paper.",

author = "{Deciphering Developmental Disorders (DDD) Study} and Joanna Kennedy and David Goudie and Edward Blair and Kate Chandler and Shelagh Joss and Victoria McKay and Andrew Green and Ruth Armstrong and Melissa Lees and Benjamin Kamien and Bruce Hopper and Tan, {Tiong Yang} and Patrick Yap and Zornitza Stark and Nobuhiko Okamoto and Noriko Miyake and Naomichi Matsumoto and Ellen Macnamara and Murphy, {Jennifer L.} and Elizabeth McCormick and Hakon Hakonarson and Falk, {Marni J.} and Dong Li and Patrick Blackburn and Eric Klee and Dusica Babovic-Vuksanovic and Susan Schelley and Louanne Hudgins and Sarina Kant and Bertrand Isidor and Benjamin Cogne and Kimberley Bradbury and Mark Williams and Chirag Patel and Helen Heussler and Celia Duff-Farrier and Phillis Lakeman and Ingrid Scurr and Usha Kini and Mariet Elting and Margot Reijnders and Janneke Schuurs-Hoeijmakers and Mohamed Wafik and Anne Blomhoff and Ruivenkamp, {Claudia A. L.} and Esther Nibbeling and Dingemans, {Alexander J. M.} and Douine, {Emilie D.} and Nelson, {Stanley F.} and Maja Hempel",

year = "2020",

month = nov,

doi = "10.1038/s41436-020-00944-7",

language = "English",

volume = "22",

pages = "1920",

journal = "Genetics in Medicine",

issn = "1098-3600",

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Deciphering Developmental Disorders (DDD) Study, Kennedy, J, Goudie, D, Blair, E, Chandler, K, Joss, S, McKay, V, Green, A, Armstrong, R, Lees, M, Kamien, B, Hopper, B, Tan, TY, Yap, P, Stark, Z, Okamoto, N, Miyake, N, Matsumoto, N, Macnamara, E, Murphy, JL, McCormick, E, Hakonarson, H, Falk, MJ, Li, D, Blackburn, P, Klee, E, Babovic-Vuksanovic, D, Schelley, S, Hudgins, L, Kant, S, Isidor, B, Cogne, B, Bradbury, K, Williams, M, Patel, C, Heussler, H, Duff-Farrier, C, Lakeman, P, Scurr, I, Kini, U, Elting, M, Reijnders, M, Schuurs-Hoeijmakers, J, Wafik, M, Blomhoff, A, Ruivenkamp, CAL, Nibbeling, E, Dingemans, AJM, Douine, ED, Nelson, SF & Hempel, M 2020, 'Correction: KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants', Genetics in Medicine, vol. 22, no. 11, pp. 1920. https://doi.org/10.1038/s41436-020-00944-7

TY - JOUR

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T2 - KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants

AU - Deciphering Developmental Disorders (DDD) Study

AU - Kennedy, Joanna

AU - Goudie, David

AU - Blair, Edward

AU - Chandler, Kate

AU - Joss, Shelagh

AU - McKay, Victoria

AU - Green, Andrew

AU - Armstrong, Ruth

AU - Lees, Melissa

AU - Kamien, Benjamin

AU - Hopper, Bruce

AU - Tan, Tiong Yang

AU - Yap, Patrick

AU - Stark, Zornitza

AU - Okamoto, Nobuhiko

AU - Miyake, Noriko

AU - Matsumoto, Naomichi

AU - Macnamara, Ellen

AU - Murphy, Jennifer L.

AU - McCormick, Elizabeth

AU - Hakonarson, Hakon

AU - Falk, Marni J.

AU - Li, Dong

AU - Blackburn, Patrick

AU - Klee, Eric

AU - Babovic-Vuksanovic, Dusica

AU - Schelley, Susan

AU - Hudgins, Louanne

AU - Kant, Sarina

AU - Isidor, Bertrand

AU - Cogne, Benjamin

AU - Bradbury, Kimberley

AU - Williams, Mark

AU - Patel, Chirag

AU - Heussler, Helen

AU - Duff-Farrier, Celia

AU - Lakeman, Phillis

AU - Scurr, Ingrid

AU - Kini, Usha

AU - Elting, Mariet

AU - Reijnders, Margot

AU - Schuurs-Hoeijmakers, Janneke

AU - Wafik, Mohamed

AU - Blomhoff, Anne

AU - Ruivenkamp, Claudia A. L.

AU - Nibbeling, Esther

AU - Dingemans, Alexander J. M.

AU - Douine, Emilie D.

AU - Nelson, Stanley F.

AU - Hempel, Maja

PY - 2020/11

Y1 - 2020/11

N2 - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

AB - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

UR - http://www.scopus.com/inward/record.url?scp=85089491461&partnerID=8YFLogxK

U2 - 10.1038/s41436-020-00944-7

DO - 10.1038/s41436-020-00944-7

M3 - Article

C2 - 32814847

SN - 1098-3600

VL - 22

SP - 1920

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 11

ER -

Correction: KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants

Abstract

ASJC Scopus subject areas

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KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants

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