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Very high penetrance and occurrence of Leber’s hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation

机译：在大汉族谱系中携带ND4 G11778A突变的大汉族血栓病变，莱伯遗传视神经病变非常高

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Xiangtian Zhou; Hongxing Zhang; Fuxin Zhao; Yanchun Ji; Yi Tong; Juanjuan Zhang; Yu Zhang; Li Yang; Yaping Qian; Fan Lu; Jia Qu; Min-Xin Guan;
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1. Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation. [J] . Zhou X, Zhang H, Zhao F, Molecular genetics and metabolism . 2010,第4期

机译：在一个携带ND4 G11778A突变的汉族大谱系中，Leber的外显率很高，并且发生了Leber的遗传性视神经病变。
2. Extremely Low Penetrance of Leber's Hereditary Optic Neuropathy in 8 Han Chinese Families Carrying the ND4 G11778A Mutation [J] . Jia Qu, Xiangtian Zhou, Juanjuan Zhang Ophthalmology . 2009,第3期

机译：携带ND4 G11778A突变的8个汉族家庭的Leber遗传性视神经病极低穿透性
3. The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation. [J] . Qian Y, Zhou X, Liang M, Mitochondrion . 2011,第6期

机译：复合物III活性的改变可能导致Leber遗传性视神经病在患有ND4 G11778A突变的中国家庭中的高外显率。
4. MUTATION ANALYSIS OF EXON 7 OF THE MSH2 GENE IN PATIENTS WITH SUSPECTED HEREDITARY GASTROINTESTINAL CANCER IN CHINA [C] . Yimei Fan, Huan Zhang, Jin Dai, 第四届国际后基因组生命科学技术学术论坛 . 2006

机译：中国怀疑遗传性胃肠病患者MSH2基因第7外显子突变分析
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. Very high penetrance and occurrence of Leber’s hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation [O] . Xiangtian Zhou, Hongxing Zhang, Fuxin Zhao, -1

机译：在大中国汉族血统携带ND4 G11778a突变非常高的渗透率和发生Leber遗传性视神经病变
7. Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation [O] . Jia Qu, Xiangtian Zhou, Fuxin Zhao, 2010

机译：Leber的十个汉族遗传神经病变的低渗透载有ND6 T11484C突变的汉族家庭

Very high penetrance and occurrence of Leber’s hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation

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