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Query Trace: Optic Atrophy and ND5[orginal query]

Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia. Acta ophthalmologica 2013 Nov 91 (7): 630-4. Korkiamäki Paula, Kervinen Marko, Karjalainen Karoliina, Majamaa Kari, Uusimaa Johanna, Remes Anne Similar articles in PubMed
Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation. American journal of human genetics 2008 Dec 83 (6): 760-8. Ji Yanli, Zhang A-Mei, Jia Xiaoyun, Zhang Ya-Ping, Xiao Xueshan, Li Shiqiang, Guo Xiangming, Bandelt Hans-Jürgen, Zhang Qingjiong, Yao Yong-Ga Similar articles in PubMed
The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-White. European journal of human genetics : EJHG 2007 Feb 15 (2): 155-61. Ruiter E Mariken, Siers Marloes H, van den Elzen Christa, van Engelen Baziel G, Smeitink Jan A M, Rodenburg Richard J, Hol Frans Similar articles in PubMed