Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Atrophy and ND5[original query] |
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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 |
Mitochondrial genome analysis of primary open angle glaucoma patients. PloS one 2013 8 (8): e70760. Banerjee Deblina, Banerjee Antara, Mookherjee Suddhasil, Vishal Mansi, Mukhopadhyay Arijit, Sen Abhijit, Basu Analabha, Ray Kun |
MELAS/LS Overlap Syndrome Associated With Mitochondrial DNA Mutations: Clinical, Genetic, and Radiological Studies. Frontiers in neurology 2021 5 12 648740. Wei Yanping, Huang Yan, Yang Yingmai, Qian M |
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