<i>De novo</i> and inherited variants in <i>DDX39B</i> cause a Novel Syndrome Characterized by Neurodevelopmental Delay, Short Stature, and Congenital HypotoniaKevin T. Booth, Francesco Vetrini, Sharayu Jangam et al.|medRxiv|2023Cited by 1
P588: De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome characterized by hypotonia, epilepsy, and short statureKevin T. Booth, Francesco Vetrini, Lorenzo Graziani et al.|Genetics in Medicine Open|2024Cited by 0