Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant

Eliane Beauregard-Lacroix, Guillermo Pacheco-Cuellar, Norbert F Ajeawung, Jessica Tardif, Klaus Dieterich, Tabib Dabir, Dina Vind-Kezunovic, Susan M White, Denes Zadori, Claudia Castiglioni, Lisbeth Tranebjærg, Pernille Mathiesen Tørring, Ed Blair, Marzena Wisniewska, Maria Vittoria Camurri, Yolande van Bever, Sirinart Molidperee, Juliet Taylor, Alexandre Dionne-Laporte, Sanjay M SisodiyaRaoul C M Hennekam, Philippe M Campeau

Abstract

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

Original languageEnglish
Publication dateJan 2021
Edition1
Volume23
Number of pages1
DOIs
Publication statusPublished - Jan 2021
SeriesGenetics in medicine : official journal of the American College of Medical Genetics
ISSN1098-3600

Fingerprint

Dive into the research topics of 'Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant'. Together they form a unique fingerprint.

Cite this