(Q21124567)
English
autosomal recessive spinocerebellar ataxia 14
Human disease
- Autosomal recessive cerebellar ataxia-cognitive defect syndrome
- Autosomal recessive spinocerebellar ataxia type 14
- Ataxie spinocérébelleuse à début infantile avec retard psychomoteur
- SPARCA1
- Spinocerebellar Ataxia, Autosomal Recessive type 14
- SCAR14
- Cerebellar Ataxia, Autosomal Recessive, Spectrin-Associated, 1
- Spectrin-associated autosomal recessive cerebellar ataxia type 1
- Infantile-onset spinocerebellar ataxia-psychomotor delay syndrome
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14; SCAR14
- SPARCA
- Spectrin-associated autosomal recessive cerebellar ataxia
Statements
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Identifiers
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