Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy-Reference-Cited by-同舟云学术

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Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy

Published:1998-01 Issue:4 Volume:17 Page:403-408
ISSN:0271-3683
Container-title:Current Eye Research
language:en
Short-container-title:Current Eye Research

Author:

Mashima Yukihiko,Yamada Keiko,Wakakura Masato,Kigasawa Kazuteru,Kudoh Jun,Shimizu Nobuyoshi,Oguchi Yoshihisa

Publisher

Informa UK Limited

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Link

http://www.tandfonline.com/doi/pdf/10.1080/02713689808951221

Reference31 articles.

1. Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases

2. Leber's Hereditary Optic Neuropathy

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1. Poor visual prognosis of Asian patients with 3460 mitochondrial DNA mutation in Leber's hereditary optic neuropathy;Canadian Journal of Ophthalmology;2024-04

2. Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy;Scientific Reports;2024-03-08

3. Leber’s hereditary optic neuropathy;Rinsho Shinkeigaku;2024

4. Oxidative Stress: A Suitable Therapeutic Target for Optic Nerve Diseases?;Antioxidants;2023-07-20

5. Mitochondrial DNA variants in a cohort from Argentina with suspected Leber’s hereditary optic neuropathy (LHON);PLOS ONE;2023-02-24

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