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48 积分 2026-08-03 加入
Mitochondrial processes are impaired in hereditary inclusion body myopathy
1小时前
已完结
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
3天前
已完结
Huntingtin protein in health and Huntington’s disease: Molecular mechanisms, pathology and therapeutic strategies
1个月前
已完结
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