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Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca(2+) overload
"Transforma Page 90 and 91: Choi K, Kim Y, Park J, Park CK, Kim Page 92 and 93: Chung H-H, Lee J-B, Chung Y-H, and Page 94 and 95: 106(34):14728-14733
When covered, GLP-1s are typically subject to utilization controls such as prior authorization, which can further limit access
Glutathione: c trong danh sch thnh phn tham kho ca sn phm
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