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机译:Dysferlin突变和线粒体功能障碍
Newcastle Univ Inst Neurosci Wellcome Trust Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH;
Newcastle Univ Inst Neurosci Wellcome Trust Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH;
Newcastle Univ Inst Neurosci Wellcome Trust Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH;
Newcastle Univ Inst Neurosci Wellcome Trust Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH;
Newcastle Univ Inst Neurosci Wellcome Trust Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH;
Newcastle Univ Inst Neurosci Wellcome Trust Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH;
Newcastle Tyne Hosp NHS Fdn Trust Rare Dis Advisory Grp Muscle Immunoanal Unit Serv Rare;
Newcastle Univ Inst Neurosci Wellcome Trust Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH;
Newcastle Univ Inst Neurosci Wellcome Trust Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH;
Dysferlin; Mitochondria; LGMD2B; Immunofluorescence; Histochemistry; Cytochrome c oxidase deficiency;
机译:dysferlin突变与线粒体功能障碍
机译:TIMM50 TIMM50的突变通过针对线粒体生理学的关键方面而导致严重的线粒体功能障碍
机译:多功能机线粒体功能障碍不是MFN2突变的主要特征(回复:CMT2由于纯合的MFN2变体是多核线粒体障碍)
机译:线粒体DNA突变和疾病
机译:线粒体DNA突变在少肌症中的作用:对线粒体“恶性循环”理论和细胞凋亡的影响。
机译:dysferlin突变与线粒体功能障碍
机译:dysferlin突变与线粒体功能障碍