Clinical phenotype and the G11778A mutation of mitochondrial DNA in patients with Leber's hereditary optic neuropathy in Taiwan

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Neuro-Ophthalmology, Vol. 26, Iss. 4, 2001-12 ,pp. : 207-216

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The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy

By Chinnery P.F.  

Brain, Vol. 124, Iss. 1, 2001-01 ,pp. : 209-218

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Multicenter study on the frequency of three primary mutations of mitochondrial DNA in Japanese pedigrees with Leber's hereditary optic neuropathy: comparison with American and British counterparts

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Neuro-Ophthalmology, Vol. 22, Iss. 3, 1999-10 ,pp. : 187-193

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Visual prognosis of Leber's hereditary optic neuropathy with 14484/ND6 mutation in Koreans

By Hwang Jeong-Min   Lee Jong Jae   Chang Bong Leen   Park Sung Sup  

Neuro-Ophthalmology, Vol. 24, Iss. 3, 2000-10 ,pp. : 421-426

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OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion

By Zanna Claudia  

Brain, Vol. 131, Iss. 2, 2008-02 ,pp. : 352-367

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