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searching for SCN1B 4 found (16 total)

alternate case: sCN1B

Dravet syndrome (4,117 words) [view diff] exact match in snippet view article find links to article

there is likely a more polygenic cause of Dravet syndrome in these cases. - SCN1B: This gene encodes the beta-1 subunit of the sodium ion channel, which regulates

Idiopathic generalized epilepsy (678 words) [view diff] exact match in snippet view article find links to article

the sodium channel α subunit genes SCN1A and SCN2A and the β subunit gene SCN1B. Mutations in the GABAA receptor γ subunit GABRG1 are also causative for

Sudden unexpected death in epilepsy (2,710 words) [view diff] exact match in snippet view article find links to article

CACNA1C have been identified with LQT8. The sodium ion channel genes SCN1A, SCN1B, SCN2A, and SCN8A and the potassium channel KCNA1 have been implicated in

Lori L. Isom (593 words) [view diff] case mismatch in snippet view article find links to article

Isom L (2019). "Delayed maturation of GABAergic signaling in the Scn1a and Scn1b mouse models of Dravet Syndrome". Scientific Reports. 9 (1): 6201. Bibcode:2019NatSR