Associated Papers
Human clinical mutations in mitochondrially encoded subunits of Complex I can be successfully modeled in E. coli.
Zhang F et al.
Mitochondrion, 2022
[Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial ND1 T3866C mutation].
Liu Y et al.
Yi Chuan = Hereditas, 2010
Pathogenic mitochondrial DNA mutations in protein-coding genes.
Wong LJ
Muscle & Nerve, 2007
[Analysis of mitochondrial gene mutations in pedigrees of Leber's hereditary optic neuropathy].
Lin L et al.
Yi Chuan = Hereditas, 2003
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