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