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.
-д хадгалсан:
| Үндсэн зохиолч: | |
|---|---|
| Формат: | Artigo |
| Хэл сонгох: | Inglês |
| Хэвлэсэн: |
Pediatric Neurology Briefs Publishers
2009-05-01
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| Цуврал: | Pediatric Neurology Briefs |
| Нөхцлүүд: | |
| Онлайн хандалт: | https://www.pediatricneurologybriefs.com/articles/270 |
| Шошгууд: |
Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!
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