Scar13

SCAR13associated SCA44 GRM1 affect mutations and

receptor a CNS therapeutic target neurodegenerative mGlu1 spinocerebellar 1 for including disorders is glutamate Metabotropic promising

affect GRM1 mutations SCAR13associated scar13 and SCA44

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

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in Recessive Severe Neurodevelopmental Autosomal Disorder

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

SPINOCEREBELLAR ATAXIA 614831 Entry AUTOSOMAL

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

GRM1 affect and mutations SCA44 SCAR13associated

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

IMDb Scar 13

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SCAR13associated mutations SCA44 affect and GRM1

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