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autosomal recessive spinocerebellar ataxia 13(Q21124572)

From Wikidata
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
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    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

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