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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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Pediatric Neurology Briefs Publishers
2009-05-01
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| coleção: | Pediatric Neurology Briefs |
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| Acesso em linha: | https://www.pediatricneurologybriefs.com/articles/270 |
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