Updates are available Erratum dated 2020-05-01
Click to view Erratum: https://doi.org/10.1038/s41436-020-0784-7
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Authors
Cuvertino, Sara
Hartill, Verity
Colyer, Alice
Garner, Terence
Nair, Nisha
Al-Gazali, Lihadh
Canham, Natalie
Faundes, Victor
Flinter, Frances
Hertecant, Jozef
Holder-Espinasse, Muriel
Jackson, Brian
Lynch, Sally Ann
Nadat, Fatima
Narasimhan, Vagheesh M.
Peckham, Michelle
Sellers, Robert
Seri, Marco
Montanari, Francesca
Southgate, Laura
Squeo, Gabriella Maria
Trembath, Richard
van Heel, David
Venuto, Santina
Weisberg, Daniel
Stals, Karen
Ellard, Sian
Barton, Anne
Kimber, Susan J.
Sheridan, Eamonn
Merla, Giuseppe
Stevens, Adam
Johnson, Colin A.
Banka, Siddharth http://orcid.org/0000-0002-8527-2210
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Funding
Funding for this research was provided by:
Newlife – The Charity for Disabled Children (16-17/10, 16-17/10, 16-17/10, 16-17/10, 16-17/10)
Chile’s National Commission for Scientific and Technological Research (72160007)
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More Information
This article is maintained by: Elsevier
Article Title: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct fromKabuki syndrome
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0743-3
Content Type: article
Copyright: © 2020, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
