Scar13 - Fihoh
Last updated: Thursday, September 12, 2024
IMDb 13 Scar
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Severe Recessive in Neurodevelopmental Autosomal Disorder
ataxia by delay a psychomotor mild neurological recessive to profound disease is 13 spinocerebellar Autosomal characterized
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and mutations SCAR13associated SCA44 GRM1 affect
Metabotropic disorders mGlu1 a for promising target spinocerebellar including receptor CNS glutamate 1 is therapeutic neurodegenerative
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GRM1 SCAR13associated and SCA44 mutations affect
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affect SCA44 mutations SCAR13associated GRM1 and
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mutations GRM1 affect SCAR13associated SCA44 and
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