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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| 042 | |a dc | ||
| 100 | 1 | 0 | |a J Gordon Millichap |e author |
| 245 | 0 | 0 | |a Repetitive Daily Blindness with Hemiplegic Migraine and SCN1A Mutations |
| 260 | |b Pediatric Neurology Briefs Publishers, |c 2009-05-01T00:00:00Z. | ||
| 500 | |a 1043-3155 | ||
| 500 | |a 2166-6482 | ||
| 500 | |a 10.15844/pedneurbriefs-23-5-4 | ||
| 520 | |a 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. | ||
| 546 | |a EN | ||
| 690 | |a familial hemiplegic migraine | ||
| 690 | |a visual symptoms | ||
| 690 | |a electroretinogram | ||
| 690 | |a Pediatrics | ||
| 690 | |a RJ1-570 | ||
| 690 | |a Neurology. Diseases of the nervous system | ||
| 690 | |a RC346-429 | ||
| 655 | 7 | |a article |2 local | |
| 786 | 0 | |n Pediatric Neurology Briefs, Vol 23, Iss 5, Pp 36-36 (2009) | |
| 787 | 0 | |n https://www.pediatricneurologybriefs.com/articles/270 | |
| 787 | 0 | |n https://doaj.org/toc/1043-3155 | |
| 787 | 0 | |n https://doaj.org/toc/2166-6482 | |
| 856 | 4 | 1 | |u https://doaj.org/article/e61218acdc9b47dab3019fbb1502c8c5 |z Connect to this object online. |