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机译:Ndufaf8的病原双等等位基因突变导致Leigh综合征与孤立的综合体I缺乏
Newcastle Univ Wellcome Ctr Mitochondrial Res Framlington Pl Newcastle Upon Tyne NE2 4HH Tyne &
Morgridge Inst Res Madison WI 53715 USA;
Goethe Univ Funct Prote D-60590 Frankfurt Germany;
Baylor Coll Med Dept Mol &
Human Genet Houston TX 77030 USA;
Morgridge Inst Res Madison WI 53715 USA;
Newcastle Univ Wellcome Ctr Mitochondrial Res Framlington Pl Newcastle Upon Tyne NE2 4HH Tyne &
Newcastle Univ Wellcome Ctr Mitochondrial Res Framlington Pl Newcastle Upon Tyne NE2 4HH Tyne &
St Marys Hosp Manchester Ctr Genom Med Oxford Rd Manchester M13 9WL Lancs England;
Manchester Univ Hosp NHS Fdn Trust Royal Manchester Childrens Hosp Acad Unit Paediat Radiol;
Childrens Natl Hosp Rare Dis Inst Washington DC 20010 USA;
Childrens Natl Hosp Rare Dis Inst Washington DC 20010 USA;
DRK Kinderklin Siegen Wellersbergstr 60 D-57072 Siegen Germany;
Newcastle Univ Wellcome Ctr Mitochondrial Res Framlington Pl Newcastle Upon Tyne NE2 4HH Tyne &
Tech Univ Munich Inst Human Genet D-81675 Munich Germany;
Tech Univ Munich Inst Human Genet D-81675 Munich Germany;
Baylor Coll Med Dept Mol &
Human Genet Houston TX 77030 USA;
Goethe Univ Funct Prote D-60590 Frankfurt Germany;
Morgridge Inst Res Madison WI 53715 USA;
Newcastle Univ Wellcome Ctr Mitochondrial Res Framlington Pl Newcastle Upon Tyne NE2 4HH Tyne &
机译:Ndufaf8的病原双等等位基因突变导致Leigh综合征与孤立的综合体I缺乏
机译:ND3基因中新的线粒体DNA复发突变与孤立的复合物I缺乏症相关,引起Leigh综合征和肌张力障碍。
机译:NADH脱氢酶5基因中的线粒体DNA G13513A MELAS突变是Leigh-like综合征的常见原因,伴有孤立的复合体I缺陷。
机译:GIY222ISP和SER379LYS - Nutef因子X基因突变在Sewere FX缺陷中 - Greifswasd注册表I先天性缺乏
机译:在李氏综合征果蝇模型中鉴定抑制神经变性的突变的候选基因
机译:Ndufaf8的病原双等异位突变引起Leigh综合征孤立的综合体I缺乏
机译:Ndufaf8的病原双等异位突变引起Leigh综合征,孤立的综合体I缺乏