Repetitive Daily Blindness with Hemiplegic Migraine and SCN1A Mutations
DOI:
https://doi.org/10.15844/pedneurbriefs-23-5-4Keywords:
Familial Hemiplegic Migraine, Visual Symptoms, ElectroretinogramAbstract
Two novel SCN1A mutations are identified in two unrelated families with familial hemiplegic migraine and a unique phenotype of elicited repetitive daily blindness, in a report from Hopital Lariboisiere, and other centers in Paris, France, and Geneva, Switzerland.Published
2009-05-01
Issue
Section
Headache Disorders
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Copyright (c) 2009 The Author(s)
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