<i>De novo</i> and inherited variants in <i>DDX39B</i> cause a Novel Syndrome Characterized by Neurodevelopmental Delay, Short Stature, and Congenital Hypotonia
Kevin T. Booth(Indiana University School of Medicine), Francesco Vetrini(Indiana University – Purdue University Indianapolis), Ty C. Lynnes(Indiana University – Purdue University Indianapolis), Kayla Treat(Indiana University – Purdue University Indianapolis), Martin M.C. Chui(University of Hong Kong), Celanie K. Christensen(Riley Hospital for Children), Kerry White(Indiana University Health), Lorenzo Graziani(Scuola Internazionale Superiore di Studi Avanzati), Hugo J. Bellen(Baylor College of Medicine), Brian Hon‐Yin Chung(Long Island Jewish Medical Center), Sharayu Jangam(Baylor College of Medicine), Christopher Chun Yu Mak(Chinese University of Hong Kong), Daniela Iancu(Wessex Regional Genetics Laboratory), Erin Conboy(Indiana University – Purdue University Indianapolis), Shinya Yamamoto(Kyoto University), Remo Sanges(Stazione Zoologica Anton Dohrn), Alessia Soldano(VIB-KU Leuven Center for Cancer Biology), Sally Ann Lynch(University College Dublin), Michael F. Wangler(Baylor College of Medicine), Anna Y. Kwong(University of Hong Kong), Julia Batista(University of Plymouth), Shelag K. Joss(Queen Elizabeth University Hospital), Oguz Kanca(University of California, Los Angeles), Mandy Ho‐Yin Tsang(University of Hong Kong), Sureni V. Mullegama
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