IndraLab

Statements

SCN1A binds NAV1. 2 / 2

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sparser

"A recent report of 9 patients with an early profound form of SMEI xref reported one patient with an Nav1.1-p."

29466837

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sparser

"Mutations of the gene SCN1A (which encodes Nav1.1) in the nervous system have been associated with human inherited epileptic syndromes and familial hemiplegic migraine, suggesting that Nav1.1 might participate in the genesis of migraine ( xref ; xref )."

21714116

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IndraLab

Statements

SCN1A binds NAV1. 2 / 2

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