Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload. - Li H; Ma Q; Xue Y; Cai L; Bao L; Hong L; Zeng Y; Huang SZ; Finnell RH; Zeng F (Science China. Life sciences, 2025)