Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation-Reference-Cited by-同舟云学术

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Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation

Published:1994-09 Issue:3 Volume:94 Page:265-270
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Oostra Roelof-Jan,Bolhuis Pieter A.,Zorn-Ende Ina,de Kok-Nazaruk Maryla M.,Bleeker-Wagemakers Elisabeth M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00208281.pdf

Cited by 31 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. MCAT Mutations Cause Nuclear LHON-like Optic Neuropathy;Genes;2021-04-02

2. Oldies but Goldies mtDNA Population Variants and Neurodegenerative Diseases;Frontiers in Neuroscience;2018-10-12

3. LHON mutations in Italian patients affected by multiple sclerosis;Acta Neurologica Scandinavica;2009-01-29

4. On the many faces of Leber hereditary optic neuropathy;Clinical Genetics;2008-06-28

5. Leber's hereditary optic neuropathy: A multifactorial disease;Progress in Retinal and Eye Research;2006-07

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