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Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload

Crossref DOI link: https://doi.org/10.1007/s11427-023-2549-2

Published Online: 2024-10-11

Published Print: 2025-02

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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