De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females
R. Webster; M.T. Cho; K. Retterer; F. Millan; C. Nowak; J. Douglas; A. Ahmad; G.V. Raymond; M.R. Johnson; A. Pujol; A. Begtrup; D. McKnight; O. Devinsky; W.K. Chung
Author Information: Department of Medicine
|Checking for direct PDF access through Ovid|
Abstract unavailable for this article.