Scar13
Last updated: Tuesday, May 20, 2025
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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
mGlu1 SCA44 function mGlu1 Mutant Keywords spinocerebellar naturally allosteric Running Title modulation mutations occurring glutamate ataxia
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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