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- W2034785871 abstract "Mutations of the SCN1A subunit of the sodium channel is a cause of genetic epilepsy with febrile seizures plus (GEFS(+) ) in multiplex families and accounts for 70-80% of Dravet syndrome (DS). DS cases without SCN1A mutation inherited have predicted SCN9A susceptibility variants, which may contribute to complex inheritance for these unexplained cases of DS. Compared with controls, DS cases were significantly enriched for rare SCN9A genetic variants. None of the multiplex febrile seizure or GEFS(+) families could be explained by highly penetrant SCN9A mutations." @default.
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- W2034785871 date "2013-07-29" @default.
- W2034785871 modified "2023-10-18" @default.
- W2034785871 title "Role of the sodium channel<i>SCN9A</i>in genetic epilepsy with febrile seizures plus and Dravet syndrome" @default.
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- W2034785871 doi "https://doi.org/10.1111/epi.12323" @default.
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