Published 2009
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Repetitive Daily Blindness with Hemiplegic Migraine and SCN1A Mutations
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Abstract
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.Files
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- PNB-23-36
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2009When the item was originally created.