A novel SCN1A mutation identified in a Chinese family with familial hemiplegic migraine: A case report

Title
A novel SCN1A mutation identified in a Chinese family with familial hemiplegic migraine: A case report
Authors
Keywords
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Journal
CEPHALALGIA
Volume 37, Issue 13, Pages 1294-1298
Publisher
SAGE Publications
Online
2016-11-09
DOI
10.1177/0333102416677049

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