Scar13

Last updated: Tuesday, May 20, 2025

Scar13
Scar13

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Severe Disorder in Neurodevelopmental Recessive Autosomal

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

SCA44 mutations affect and GRM1 SCAR13associated

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AUTOSOMAL 614831 Entry ATAXIA SPINOCEREBELLAR

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

and SCA44 affect SCAR13associated GRM1 mutations

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affect SCAR13associated mutations and GRM1 SCA44

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SCAR13associated and affect mutations GRM1 SCA44

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