Repetitive Daily Blindness with Hemiplegic Migraine and SCN1A Mutations
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.
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| Format: | Book |
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Pediatric Neurology Briefs Publishers,
2009-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | 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. |
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| Item Description: | 1043-3155 2166-6482 10.15844/pedneurbriefs-23-5-4 |