De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females
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W. Chung | O. Devinsky | G. Raymond | M. Johnson | K. Retterer | D. McKnight | M. Cho | F. Millan | A. Begtrup | A. Pujol | C. Nowak | J. Douglas | R. Webster | A. Ahmad | W. Chung | M.R. Johnson