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一个患有伴有线粒体11778/ND4和4216/ND1突变的Leber遗传性视神经病变的家族。

A family with Leber's hereditary optic neuropathy with mitochondrial 11778/ND4 and 4216/ND1 mutations.

作者信息

Hwang J M

机构信息

Department of Ophthalmology, Seoul Municipal Boramae Hospital, College of Medicine Seoul National University, Korea.

出版信息

Korean J Ophthalmol. 2000 Jun;14(1):45-8. doi: 10.3341/kjo.2000.14.1.45.

Abstract

Leber's hereditary optic neuropathy (LHON) is caused by a point mutation in the mitochondrial deoxynucleic acid (mtDNA) and accounts for 30% of bilateral optic atrophy of unknown etiology. The authors found a Korean family with mtDNA mutations in the nucleotide positions (np) 11778 and np 4216. This is the first report confirming a secondary mtDNA np 4216 mutation in Koreans, as well as the first report of a Korean family harboring both primary and the secondary mutations that the authors are aware of.

摘要

Leber遗传性视神经病变(LHON)由线粒体脱氧核糖核酸(mtDNA)中的点突变引起,占病因不明的双侧视神经萎缩的30%。作者发现了一个韩国家庭,其mtDNA在核苷酸位置(np)11778和np 4216处发生了突变。这是首次证实韩国人存在继发性mtDNA np 4216突变的报告,也是作者所知的首个同时携带原发性和继发性突变的韩国家庭的报告。

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