Published 2009
| Version v1.0.0
Journal Article
Open
Repetitive Daily Blindness with Hemiplegic Migraine and SCN1A Mutations
- Creators
- Millichap, J. Gordon
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
PNB-23-36.pdf
Files
(176.0 kB)
| Name | Size | Download all |
|---|---|---|
|
md5:353b41270e69cb57f53cabe82f7edb39
|
176.0 kB | Preview Download |
Additional details
- Other
- PNB-23-36
- Created
-
2009When the item was originally created.