Spinocerebellar Ataxia 21 with Retardation
Investigators at Universite de Lille Nord de France, and other centers in France, report the identification of a novel causative gene for spinocerebellar ataxia 21, an autosomal dominant disorder, initially mapped to chromosome 7 and designated as SCA21.
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2014-11-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/68 |