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

Research output: Contribution to journalArticle

Abstract

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

Original languageEnglish
Pages (from-to)1920
Number of pages1
JournalGenetics in Medicine
Volume22
Issue number11
Early online date19 Aug 2020
DOIs
Publication statusPublished - Nov 2020

ASJC Scopus subject areas

  • Genetics(clinical)

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

    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. & Murphy, J. L. & 32 others, McCormick, E., Hakonarson, H., Falk, M. J., 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, C. A. L., Nibbeling, E., Dingemans, A. J. M., Douine, E. D., Nelson, S. F., Arboleda, V. A. (Lead / Corresponding author) & Newbury-Ecob, R. (Lead / Corresponding author), 24 Sept 2018, In: Genetics in Medicine. 21, p. 850-860 11 p.

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