Literature DB >> 2566021

Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy.

M Yoneda, S Tsuji, T Yamauchi, T Inuzuka, T Miyatake, S Horai, T Ozawa.   

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Year:  1989        PMID： 2566021     DOI： 10.1016/s0140-6736(89)92470-7

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  5 in total

1.  Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy.

Authors:  C Carducci; V Leuzzi; M Scuderi; A M De Negri; C B Gabrieli; I Antonozzi; A Pontecorvi
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

2.  An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene.

Authors:  N Howell; D McCullough
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025

Review 3.  Muscle mitochondrial DNA in encephalomyopathy and ragged red fibres: a Southern blot analysis and literature review.

Authors:  C Geny; V Cormier; C Meyrignac; P Cesaro; J D Degos; R Gherardi; A Rötig
Journal:  J Neurol       Date:  1991-06       Impact factor: 4.849

4.  Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia.

Authors:  Kang Wang; Yuji Takahashi; Zong-Liang Gao; Guo-Xiang Wang; Xian-Wen Chen; Jun Goto; Jin-Ning Lou; Shoji Tsuji
Journal:  Neurogenetics       Date:  2009-05-21       Impact factor: 2.660

Review 5.  Contribution of Mitochondrial DNA Variation to Chronic Disease in East Asian Populations.

Authors:  Dayan Sun; Yang Wei; Hong-Xiang Zheng; Li Jin; Jiucun Wang
Journal:  Front Mol Biosci       Date:  2019-11-15
  5 in total

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