Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novo” SCN1A Mutations in Children with Dravet Syndrome

Publisher： John Wiley & Sons Inc

E-ISSN： 1098-1004|36|9|861-872

ISSN： 1059-7794

Source： HUMAN MUTATION, Vol.36, Iss.9, 2015-09, pp. : 861-872

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