Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload - Hongyu Li; Qingwen Ma; Yan Xue; Linlin Cai; Liwen Bao; Lei Hong; Yitao Zeng; Shu-Zhen Huang; Richard H. Finnell; Fanyi Zeng (Science China Life Sciences, 2025)