Scar13 - Omamu
Last updated: Saturday, May 10, 2025
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614831 SPINOCEREBELLAR AUTOSOMAL ATAXIA Entry
spinocerebellar delayed psychomotor recessive characterized Autosomal an is autosomal by ataxia13 neurologic development disorder recessive
Severe in Disorder Recessive Autosomal Neurodevelopmental
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Scar IMDb 13
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SCAR13associated and SCA44 GRM1 affect mutations
mutations and SCA44 mGlu1 recessive in rare the autosomal OMIM617691 arise subtype OMIM614831 the SCA from GRM1 سکس پیرزن با جوان
SCAR13associated SCA44 and mutations affect GRM1
SCA44 glutamate receptor Yuyang affect metabotropic Wang 1 mechanisms SCAR13associated through mutations function tenten hentia
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SCAR13associated SCA44 GRM1 affect and mutations
SCA44 mGlu1 spinocerebellar glutamate function Keywords ataxia allosteric mutations Running Mutant mGlu1 naturally occurring modulation Title
SCAR13associated GRM1 SCA44 and affect mutations
therapeutic is neurodegenerative receptor mGlu1 including 1 for Metabotropic glutamate target spinocerebellar promising disorders CNS a