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Correction: DOORS syndrome and a recurrent truncating ATP6V1B2 variant.

作者信息

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

机构信息

Medical Genetics Division, Department of Pediatrics, Sainte-Justine University Hospital Center, Montreal, QC, Canada.

CHU Sainte Justine Research Center, Université de Montréal, Montreal, QC, Canada.

出版信息

Genet Med. 2021 Jan;23(1):237. doi: 10.1038/s41436-020-00969-y.

DOI:10.1038/s41436-020-00969-y
PMID:32934366
Abstract
摘要

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