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SCN1A binds FST and GABRG2. 1 / 1

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"Among all the epilepsy genes, mutations in SCN1A and GABRG2 have been strongly associated with FS and extended epilepsy syndromes like generalized epilepsy with febrile plus (GEFS+) and Dravet syndrome xref – xref ."

28505490

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IndraLab

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SCN1A binds FST and GABRG2. 1 / 1

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