Scar13

GRM1 SCA44 affect mutations SCAR13associated and

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

GRM1 and affect SCA44 mutations SCAR13associated

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

SCA44 affect and SCAR13associated mutations GRM1

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

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IMDb 13 Scar

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AUTOSOMAL Entry ATAXIA 614831 SPINOCEREBELLAR

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

in Autosomal Neurodevelopmental Severe Disorder Recessive

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

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SCAR13associated and SCA44 GRM1 mutations affect

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