spinocerebellar ataxia, autosomal recessive 13 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/614831
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Genes

1 genes associated with the spinocerebellar ataxia, autosomal recessive 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
GRM1 glutamate receptor, metabotropic 1