Scar13 - Yixuki

Last updated: Sunday, September 8, 2024

Scar13 - Yixuki
Scar13 - Yixuki

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AUTOSOMAL Entry ATAXIA 614831 SPINOCEREBELLAR

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

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Recessive Severe Autosomal Disorder Neurodevelopmental in

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

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SCA44 affect GRM1 SCAR13associated mutations and

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

mutations affect SCA44 SCAR13associated and GRM1

mutations

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in GRM1 SCA rare mGlu1 gene from OMIM617691 SCAR13 recessive encoding the autosomal arise SCA44 and subtype The the OMIM614831

GRM1 affect and SCAR13associated SCA44 mutations

function mGlu1 spinocerebellar ataxia

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

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SCAR13associated SCA44 and mutations GRM1 affect

glutamate SCA44 GRM1 mechanisms and through affect 1 SCAR13associated distinct

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