P588: De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome characterized by hypotonia, epilepsy, and short stature
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), 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), Anna Ka‐Yee Kwong(University of Dundee), Daniela Iancu(Wessex Regional Genetics Laboratory), Erin Conboy(Indiana University – Purdue University Indianapolis), Martin Man Chun Chui(Chinese University of Hong Kong), Júlia Baptista(University of Exeter), Remo Sanges(Stazione Zoologica Anton Dohrn), Alessia Soldano(VIB-KU Leuven Center for Cancer Biology), Sally Ann Lynch(University College Dublin), Shinya Yamamoto(Neurological Research Institute), Michael F. Wangler(Baylor College of Medicine), Shelag K. Joss(Queen Elizabeth University Hospital), Christopher CY Mak(University of Hong Kong), Oguz Kanca(University of California, Los Angeles), Mandy Ho‐Yin Tsang(University of Hong Kong), Sureni V. Mullegama
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