(Q21124572)
English
autosomal recessive spinocerebellar ataxia 13
Human disease
- Autosomal recessive spinocerebellar ataxia type 13
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13
- SCAR13
- Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency
- Spinocerebellar Ataxia, Autosomal Recessive type 13
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13; SCAR13
- Autosomal recessive congenital cerebellar ataxia due to metabotropic glutamate receptor 1 deficiency
Statements
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Identifiers
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