CNKSR2-related neurodevelopmental and epilepsy disorder: a cohort of 13 new families and literature review indicating a predominance of loss of function pathogenic variants
Higa, Leigh Ann, Wardley, Jennifer, Wardley, Christopher, Singh, Susan, Foster, Timothy, Shen, Joseph J
Published in BMC medical genomics (15.07.2021)
Published in BMC medical genomics (15.07.2021)
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