Article

Pathogenic SCN2A variants are associated with familial and sporadic hemiplegic migraine

2023-08-05

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Familial hemiplegic migraine is a severe autosomal dominant subtype of migraine with aura characterized by transient motor weakness during attacks. Previously identified genes <italic>CACNA1A</italic>, <italic>ATP1A2</italic>, <italic>SCN1A</italic> and <italic>PRRT2</italic> account for less than 20% of cases with hemiplegic migraine referred for genetic diagno...

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Literature Corpus work: e963ff23-b3cc-5160-ba5c-03222d687716
DOI: 10.21203/rs.3.rs-3215189/v1

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