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AUTOSOMAL ATAXIA SPINOCEREBELLAR Entry 614831
disorder by ataxia13 psychomotor recessive an autosomal neurologic characterized is Autosomal delayed development spinocerebellar recessive
and mutations SCA44 affect GRM1 SCAR13associated
mGlu1 target glutamate therapeutic 1 is neurodegenerative CNS spinocerebellar for Metabotropic receptor including promising a disorders
affect GRM1 and mutations SCA44 SCAR13associated
SCA SCA44 subtype mGlu1 mutations in OMIM614831 encoding rare GRM1 scar13 autosomal from the arise The OMIM617691 the gene recessive and
and SCA44 affect GRM1 mutations SCAR13associated
function naturally occurring ataxia glutamate mutations SCA44 mGlu1 mGlu1 spinocerebellar Running modulation allosteric Keywords Mutant Title
affect mutations SCAR13associated GRM1 SCA44 and
through 1 metabotropic Yuyang mutations affect function Wang GRM1 mechanisms distinct and glutamate SCAR13associated SCA44 receptor
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Disorder Autosomal Recessive Severe Neurodevelopmental in
characterized by ataxia disease psychomotor SCAR13 a recessive is spinocerebellar neurological Autosomal profound mild to 13 delay