Leber's hereditary optic neuropathy: mitochondrial and biochemical studies on muscle biopsies.-Reference-Cited by-同舟云学术

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Leber's hereditary optic neuropathy: mitochondrial and biochemical studies on muscle biopsies.

Published:1987-07-01 Issue:7 Volume:71 Page:531-536
ISSN:0007-1161
Container-title:British Journal of Ophthalmology
language:en
Short-container-title:British Journal of Ophthalmology

Author:

Uemura A,Osame M,Nakagawa M,Nakahara K,Sameshima M,Ohba N

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference19 articles.

1. Leber's hereditary optic atrophy;GI, I.Dukc-Elder S.Scott,1971

2. Leher's disease and variants;Went, L.N.,1972

3. Leher's disease;Imachi, J.;Acta Soc Ophthalmol Jpn,1973

4. Leher's hereditary optic atrophy: some clinical and actiological considerations;Wilson, J.;Brain

5. Neurological studies in families with Leber's optic atrophy;deWeerdt CJ, S.; LN, Went;Acta Neurol Scand,1971

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mitochondrial m.13513G>A Point Mutation in ND5 in a 16-Year-Old Man with Leber Hereditary Optic Neuropathy Detected by Next-Generation Sequencing;Journal of Pediatric Genetics;2019-05-28

2. L;Synopsis of Neurology, Psychiatry and Related Systemic Disorders;2019-05-23

3. Metabolic Myopathies;Swaiman's Pediatric Neurology;2012

4. Clinical phenotype and the G11778A mutation of mitochondrial DNA in patients with Leber’s hereditary optic neuropathy in Taiwan;Neuro-Ophthalmology;2001-01

5. Microphotometric analysis of NADH-tetrazolium reductase deficiency in fibroblasts of patients with Leber hereditary optic neuropathy;Journal of Inherited Metabolic Disease;2000-11

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