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DOORS syndrome and a recurrent truncating ATP6V1B2 variant

Éliane Beauregard‐Lacroix, G. Pacheco-Cuellar, Norbert Fonya Ajeawung, Jessica Tardif, Klaus Dieterich, Tabib Dabir, Dina Vind-Kezunovic, Susan M. White, Dénes Zádori, Claudia Castiglioni, Lisbeth Tranebjærg, Pernille Mathiesen Tørring, Ed Blair, Marzena Wiśniewska, Maria Vittoria Camurri, Yolande van Bever, Sirinart Molidperee, Juliet Taylor, Alexandre Dionne‐Laporte, Sanjay M. Sisodiya, Raoul C. M. Hennekam, Philippe M. Campeau

2020Genetics in Medicine31 citationsDOIOpen Access PDF

Topics & Concepts

DoorsMedicineGeneticsBiologyComputer scienceOperating systemGenomics and Rare DiseasesConnective tissue disorders researchGenetic Syndromes and Imprinting
DOORS syndrome and a recurrent truncating ATP6V1B2 variant | Litcius