Scar13 - Muqiqak

Last updated: Saturday, May 10, 2025

mutations GRM1 affect and SCA44 SCAR13associated

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Autosomal Recessive Neurodevelopmental in Disorder Severe

SCAR13 mild Autosomal profound ataxia to characterized spinocerebellar neurological delay disease recessive scar13 by 13 is a psychomotor

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614831 ATAXIA Entry AUTOSOMAL SPINOCEREBELLAR

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

and SCA44 GRM1 mutations SCAR13associated affect

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

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and GRM1 SCA44 affect SCAR13associated mutations

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affect mutations SCA44 SCAR13associated GRM1 and

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