(Q21124574)
English
autosomal recessive spinocerebellar ataxia 17
human disease
- Spinocerebellar Ataxia, Autosomal Recessive type 17
- Spinocerebellar ataxia autosomal recessive type 17
- SCAR17
- Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17
- autosomal recessive spinocerebellar ataxia type 17
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17
Statements
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Identifiers
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