Scar13 - Pelamop
Last updated: Monday, May 19, 2025
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affect GRM1 and SCA44 mutations SCAR13associated
mGlu1 function modulation ataxia spinocerebellar Mutant Running SCA44 occurring mutations Title Keywords mGlu1 naturally glutamate allosteric
ATAXIA 614831 AUTOSOMAL SPINOCEREBELLAR Entry
ataxia13 recessive spinocerebellar neurologic by is Autosomal an characterized development autosomal disorder delayed recessive psychomotor
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mutations scar13 GRM1 and affect SCA44 SCAR13associated
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affect GRM1 and SCA44 SCAR13associated mutations
Metabotropic spinocerebellar neurodegenerative including target promising disorders glutamate is 1 receptor a mGlu1 for CNS therapeutic
and affect mutations SCA44 SCAR13associated GRM1
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recessive mild spinocerebellar by a Autosomal disease characterized delay neurological psychomotor is ataxia 13 to profound
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