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机译:一种新的致病性M.4412G>一种与儿童发病癫痫发作相关的MT-TM线粒体DNA变体,肌病和双侧基础神经节变化
Newcastle Univ Inst Neurosci Wellcome Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH Tyne &
Wear England;
Newcastle Univ Inst Neurosci Wellcome Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH Tyne &
Wear England;
Newcastle Univ Inst Neurosci Wellcome Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH Tyne &
Wear England;
Newcastle Univ Inst Neurosci Wellcome Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH Tyne &
Wear England;
Newcastle Univ Inst Neurosci Wellcome Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH Tyne &
Wear England;
Newcastle Univ Inst Neurosci Wellcome Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH Tyne &
Wear England;
Royal Hosp Sick Children Dept Paediat Neurol Edinburgh EH9 1LF Midlothian Scotland;
NHS Natl Serv Scotland Inherited Metab Disorders Scotland Glasgow G2 6QE Lanark Scotland;
Newcastle Univ Inst Neurosci Wellcome Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH Tyne &
Wear England;
Newcastle Univ Inst Neurosci Wellcome Ctr Mitochondrial Res Newcastle Upon Tyne NE2 4HH Tyne &
Wear England;
Mitochondrial disease; Myopathy; Seizures; mtDNA variant; Basal ganglia changes; MTTM;
机译:一种新的致病性M.4412G>一种与儿童发病癫痫发作相关的MT-TM线粒体DNA变体,肌病和双侧基础神经节变化
机译:致病线粒体MT-TRNA(ALA)变体与分离的肌病唯一相关
机译:用于分配与线粒体疾病相关的八种线粒体DNA变体的致病性的单纤维研究
机译:HVI区域的线粒体DNA变体作为2型糖尿病遗传标记的候选者
机译:酿酒酵母的遗传背景和线粒体DNA聚合酶变异对线粒体基因组维持的分析
机译:新型致病性m.4412G MT-TM线粒体DNA变异与儿童发作性癫痫肌病和双侧基底神经节改变有关
机译:一种新型线粒体M.4414T> C MT-TM基因变体导致进步外部眼睑动脉杆菌和肌病