Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene.
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/genetics/article-pdf/133/1/133/34572611/genetics0133.pdf
Cited by 26 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. LEBER'S DISEASE. CLINICAL CASE;Bulletin of Siberian Medicine;2013-10-28
2. Mitochondrial DNA sequence variation is associated with free-living activity energy expenditure in the elderly;Biochimica et Biophysica Acta (BBA) - Bioenergetics;2012-09
3. OUTER RETINAL DYSFUNCTION IN A PATIENT WITH THE 15257 MITOCHONDRIAL DNA MUTATION;RETINAL Cases & Brief Reports;2011
4. Investigation on Mitochondrial tRNALeu/Lys, NDI and ATPase 6/8 in Iranian Multiple Sclerosis Patients;Cellular and Molecular Neurobiology;2007-07-06
5. Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background;American Journal of Medical Genetics;2003-05-09
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