- A family with Leber's hereditary optic neuropathy with mitochondrial 11778/ND4 and 4216/ND1 mutations
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Hwang JM
- KMID: 754273
- Korean J Ophthalmol.
- 2000 Jun;14(1):45-48.
- doi: 10.3341/kjo.2000.14.1.45
Leber's hereditary optic neuropathy (LHON) is caused by a point mutation in the mitochondrial deoxynucleic acid (mtDNA) and accounts for 30+ACU- of bilateral optic atrophy of unknown etiology. The authors... -
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- Enzyme histochemical study of germanium dioxide-induced mitochondrial myopathy in rats
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Yim SY, Lee IY, Kim TS
- KMID: 1099881
- Yonsei Med J.
- 1999 Feb;40(1):69-75.
- doi: 10.3349/ymj.1999.40.1.69
The purpose of this study were 1) to determine the earliest pathological changes of germanium dioxide (GeO2)-induced myopathy; 2) to determine the pathomechanism of GeO2-induced myopathy; and 3)... -
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