Leber's Hereditary Optic Neuropathy
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference6 articles.
1. The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations;Zou;Biochem Biophys Res Commun,2010
2. Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families;Liu;Ophthalmology,2011
3. Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic;Kong;J Hum Genet,2004
4. Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation;van Oven;Hum Mutat,2009
5. Rapid identification of mtDNA somatic mutations in gastric cancer tissues based on the mtDNA phylogeny;Bi;Mutat Res,2011
Cited by 1 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. Haplogroup Heterogeneity of LHON Patients Carrying the m.14484T>C Mutation in India;Investigative Opthalmology & Visual Science;2013-06-10
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