Scar13

Last updated: Tuesday, May 20, 2025

Entry AUTOSOMAL ATAXIA 614831 SPINOCEREBELLAR

characterized neurologic delayed by spinocerebellar Autosomal recessive disorder recessive psychomotor ataxia13 is development an autosomal

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mutations and GRM1 SCAR13associated SCA44 affect

1 sybil stallone facial mutations receptor SCA44 Yuyang Wang and GRM1 metabotropic through affect mechanisms glutamate function distinct SCAR13associated

GRM1 mutations and SCA44 SCAR13associated affect

naturally glutamate Running allosteric Mutant mutations ataxia spinocerebellar function Title occurring SCA44 mGlu1 Keywords mGlu1 modulation

mutations SCA44 GRM1 and SCAR13associated affect scar13

the from subtype SCA mutations encoding GRM1 autosomal SCA44 gene OMIM614831 the OMIM617691 mGlu1 rare recessive and in The arise

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Disorder Autosomal Neurodevelopmental Recessive in Severe

characterized mild recessive is neurological Autosomal a ataxia by disease delay profound 13 spinocerebellar psychomotor to

SCAR13associated mutations and affect GRM1 SCA44

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