Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019))

Authors

Erfan Aref-Eshghi
Jennifer Kerkhof
Victor P. Pedro
Groupe DI France
Mouna Barat-Houari
Nathalie Ruiz-Pallares
Jean Christophe Andrau
Didier Lacombe
Julien Van-Gils
Patricia Fergelot
Christéle Dubourg
Valerie Cormier-Daire
Sophie Rondeau
François Lecoquierre
Pascale Saugier-Veber
Gaël Nicolas
Gaetan Lesca
Nicolas Chatron
Damien Sanlaville
Antonio Vitobello
Laurence Faivre
Christel Thauvin-Robinet
Frederic Laumonnier
Martine Raynaud
Mariëlle Alders
Marcel Mannens
Peter Henneman
Raoul C. Hennekam
Guillaume Velasco

Document Type

Article

Publication Date

6-3-2021

Journal

American Journal of Human Genetics

Volume

108

Issue

6

First Page

1161

Last Page

1163

URL with Digital Object Identifier

10.1016/j.ajhg.2021.04.022

Abstract

(The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper originally published, the underlying cause for Hunter McAlpine syndrome was incorrectly described in Table 1. The relevant description has been changed to read “Chr5q35-qter duplication involving NSD1” in the updated Table 1 reflected here. The authors apologize for this error.