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`Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation

机译：“二级”4216 / ND1和13708 / ND5 Leber的遗传性视神经病理学线粒体DNA突变在与11778 / ND4线粒体DNA突变相关时，在体内线粒体氧化代谢中没有进一步损害

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R. Lodi;
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1. 'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation. [J] . Lodi R, Montagna P, Cortelli P, Brain: A journal of neurology . 2000,第Pta9期

机译：当与11778 / ND4线粒体DNA突变相关时，“次级” 4216 / ND1和13708 / ND5 Leber的遗传性视神经病线粒体DNA突变不会进一步损害体内线粒体的氧化代谢。
2. Phylogenetic assessment of the mitochondrial DNA displacement loop haplotype in Japanese patients with Leber's hereditary optic neuropathy harboring the mitochondrial DNA G11778A mutation. [J] . Isashiki Y, Sonoda S, Izumo S, Ophthalmic Research: Journal for Research in Experimental and Clinical Ophthalmology . 2003,第4期

机译：对日本患者携带线粒体DNA G11778A突变的Leber遗传性视神经病患者的线粒体DNA置换环单倍型进行系统发育评估。
3. Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G&A and m.14484T&C of the mitochondrial DNA [J] . Claudia B. Catarino, Uwe Ahting, Mirjana Gusic, Mitochondrion . 2017,第期

机译：Leber的遗传性视神经病变（LHON）家族的特征涉及两个主要LHON突变M.11778G＆amp; GT; GT; GT; GT; C;线粒体DNA
4. Repeated Ovarian Stimulations Induce Oxidative Damage and Mitochondrial DNA Mutations in Mouse Ovaries [C] . HSIANG-TAI CHAO, SHU-YU LEE, HORNG-MO LEE, Asian Society for Mitochondrial Research and Medicine . 2005

机译：反复卵巢刺激诱导小鼠卵巢中的氧化损伤和线粒体DNA突变
5. Biochemical and genetic characterization of mitochondrial encephalomyopathies resulting from mitochondrial-DNA (mtDNA) and nuclear DNA (nDNA) mutations. [D] . Zheng, Xianxian. 1990

机译：由线粒体DNA（mtDNA）和核DNA（nDNA）突变引起的线粒体脑肌病的生化和遗传特征。
6. Co-occurrence of m.1555AG and m.11778GA mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy [O] . Nahid Akhtar Khan, Periyasamy Govindaraj, Vuskamalla Jyothi, 2013

机译：在两个印度家庭中同时出现Leber遗传性视神经病变的m.1555A G和m.11778G A线粒体DNA突变
7. Leber's Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNA [O] . Kazuhiro Nakaso, Yoshiki Adachi, Emi Fusayasu, 2012

机译：由于线粒体DNA的G11778A和T3394C突变，Leber的遗传视神经病变与Olivocerebellar退化产生的术语

`Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation

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