机译:与ATP酶生物发生相关的PRICKLE3表现为Leber遗传性视神经病变
Wenzhou Med Univ, Sch Optometry & Ophthalmol, Wenzhou, Peoples R China;
Zhejiang Univ, Sch Med, Inst Genet, 866 Yuhangtang Rd, Hangzhou 310058, Zhejiang, Peoples R China;
Zhejiang Univ, Childrens Hosp, Div Med Genet & Genom, Sch Med, Hangzhou, Peoples R ChinaHebei Prov Eye Hosp, Dept Ophthalmol, Xingtai, Peoples R ChinaCincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA;
机译:Mitochondrial gene therapy improves respiration, biogenesis, and transcription in G11778A leber's hereditary optic neuropathy and T8993G leigh's syndrome cells
机译:The Leber hereditary optic neuropathy 14,484 mutation and X-linked adrenoleukodystrophy: a possible modifier of phenotypic expression?
机译:X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant
机译:prickle3与Atpase生物生成的表现形式莱伯的遗传视神经病变
机译:Coenzyme Q10 Therapy in Hereditary motor sensory Neuropathy Type VI with Novel mitofusin 2 mutation