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Leber's Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNA

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

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Kazuhiro Nakaso; Yoshiki Adachi; Emi Fusayasu; Koji Doi; Keiko Imamura; Kenichi Yasui; Kenji Nakashima;
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年度 2012
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1. Leber's Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNA [J] . Nakaso Kazuhiro, Adachi Yoshiki, Fusayasu Emi, Journal of Clinical Neurology . 2012,第3期

机译：由于线粒体DNA中的G11778A和T3394C突变而导致的Leber遗传性视神经病变伴小脑小脑变性
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. Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA [J] . Qiao Chen, Wei Tanwei, Hu Bo, Molecular medicine reports . 2015,第2aPta2期

机译：Leber遗传性视神经病变的两个家族，线粒体DNA中带有单倍群H2a2a1的G11778A和T14502C突变
4. Mitochondrial DNA Mutations and Diseases [C] . Lee-Jun C. Wong Annual Meeting of the American College of Veterinary Pathologists . 2014

机译：线粒体DNA突变和疾病
5. A Review of Leber Hereditary Optic Neuropathy and Stargardt's Disease: Comfort Level of Genetic Counselors in Dealing with Patients with these two Disorders [D] . Pani, Blerta 2011

机译：Leber遗传性视神经病变和Stargardt病的综述：遗传咨询员在应对这两种疾病时的舒适度
6. Lebers 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：线粒体DNA中的G11778A和T3394C突变导致Leber遗传性视神经病变伴小脑小脑变性
7. Brain stem lesion in mitochondrial DNA G11778A mutation of Leber's hereditary optic neuropathy [O] . Yan-Ting Chen, Wei-Liang Chen, San-Ni Chen, 2015

机译：Leber遗传性视神经病变线粒体DNa G11778a突变的脑干病变

Leber's Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNA

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