Literature DB >> 11501521

Optic neuropathy and cerebellar ataxia associated with a rare missense variation (A14510G) of mitochondrial DNA.

Y Isashiki, N Ohba, S Izumo.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2001        PMID： 11501521      PMCID： PMC1724068          DOI： 10.1136/bjo.85.8.1007b

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN： 0007-1161            Impact factor:   4.638


× No keyword cloud information.
  2 in total

1.  Leber's hereditary optic neuropathy with the 3434, 9011 mitochondrial DNA point mutation.

Authors:  Kyoko Shidara; Masato Wakakura
Journal:  Jpn J Ophthalmol       Date:  2011-12-20       Impact factor: 2.447

2.  Mitochondrial DNA mutations with Leber's hereditary optic neuropathy in Japanese patients with open-angle glaucoma.

Authors:  Yoko Inagaki; Yukihiko Mashima; Nobuo Fuse; Yuichiro Ohtake; Takuro Fujimaki; Takeo Fukuchi
Journal:  Jpn J Ophthalmol       Date:  2006 Mar-Apr       Impact factor: 2.211
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.