(Q21124560)
English
autosomal recessive spinocerebellar ataxia 18
Human disease
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18; SCAR18
- SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18
- Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency
- Autosomal recessive congenital cerebellar ataxia due to ionotropic glutamate receptor delta-2 subunit deficiency
- Spinocerebellar Ataxia, Autosomal Recessive type 18
- SCAR18
- autosomal recessive spinocerebellar ataxia type 18
Statements
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Identifiers
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