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| Pediatric Neurology Briefs: Volume 28, Issue 11 |
Spinocerebellar Ataxia 21 with Retardation Open Access (recommended)
Descriptions
- Resource type(s)
- Article
- Keyword
- TMEM240
SCA21
Retardation
- Rights
- Attribution 4.0 International
- Creator
-
Millichap, John J.
Millichap, J. Gordon
- Abstract
-
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.
- Publisher
-
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
- Date Created
-
2014
- Original Identifier
- PNB-2014-28-11-1
- Language
- English
- Subject: MESH
-
Brain Diseases
Infant
Pediatrics
Nervous System Diseases
Child Development
Neurology
Neurosurgery
Child
- DOI
-
10.15844/pedneurbriefs-28-11-1
File Details
- File Properties
-
Mime type: application/pdf
File size: 105.8 kB