Associated Papers
Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation.
Xu XB et al.
Chinese Medical Journal, 2019
Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family.
Wang J et al.
Molecular Genetics and Metabolism, 2009
[Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].
Zhang XA et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2005
Clinical and molecular findings in children with complex I deficiency.
Bugiani M et al.
Biochimica Et Biophysica Acta, 2004
Select a paper to view details