eP410: De novo missense variants in DDX39B cause a novel syndrome characterized by neurodevelopmental delay, short stature and congenital hypotonia

Kayla Treat(Indiana University – Purdue University Indianapolis), Francesco Vetrini(Indiana University – Purdue University Indianapolis), Martin MC. Chui(University of Hong Kong), Celanie K. Christensen(Riley Hospital for Children), Kerry White(Indiana University Health), Hugo J. Bellen(Baylor College of Medicine), Mandy HY. Tsang(University of Hong Kong), Sharayu Jangam(Baylor College of Medicine), Brian HY. Chung(University of Hong Kong), Erin Conboy(Indiana University – Purdue University Indianapolis), Júlia Baptista(University of Exeter), Sally Ann Lynch(University College Dublin), Shinya Yamamoto(Neurological Research Institute), Michael F. Wangler(Baylor College of Medicine), Kristy Jay(Baylor College of Medicine), Liz Y. P. Yuen(Duchess of Kent Children's Hospital), Oguz Kanca(University of California, Los Angeles)
Genetics in Medicine
March 1, 2022
Cited by 0


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