首页> 美国卫生研究院文献>The British Journal of Ophthalmology >Lebers hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutation.
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Lebers hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutation.

机译:Leber的遗传性视神经病变:异质性在3460 ND1突变家族的LHON表达中可能很重要。

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摘要

AIM: To assess the effect of heteroplasmy on the expression of Leber's hereditary optic neuropathy (LHON) in a large family with the 3460 LHON mutation. METHODS: Mutation detection was performed by restriction enzyme digestion of polymerase chain reaction (PCR) products. Heteroplasmy was estimated by quantitation of wild type:mutant product ratios. RESULTS: There is a significant association between levels of mutant mtDNA and manifestation of the disease phenotype. CONCLUSION: As a high proportion of families with the 3460 mutation demonstrate heteroplasmy; this is likely to be a significant factor in disease expression.
机译:目的:评估异质性对具有3460 LHON突变的大家族Leber遗传性视神经病变(LHON)表达的影响。方法:通过限制性酶消化聚合酶链反应(PCR)产物进行突变检测。通过定量野生型:突变产物的比率来估计异质性。结果:突变线粒体DNA水平与疾病表型的表现之间有显着的关联。结论:3460突变的家庭中有很大一部分表现出异质性。这很可能是疾病表达的重要因素。

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