(Q21124571)
English
autosomal recessive spinocerebellar ataxia 2
human disease
- SCAR2
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2
- Cerebellar Granular Cell Hypoplasia and Mental Retardation, Congenital
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2
- Cerebellar Hypoplasia, Nonprogressive Norman Type
- Cpd 3
- Autosomal recessive spinocerebellar ataxia type 2
- Cerebelloparenchymal Disorder 3
- Autosomal recessive cerebelloparenchymal disorder type 3
Statements
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4 references
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Identifiers
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