Tomoko Myint

An additional mitochondrial tRNAIle point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy

Frank Merante, Tomoko Myint, Ingrid Tein et al. · Human Mutation · 1996 · 109 citations

Life Sciences, Genetics, Molecular Genetics +16

Clinical variability in maternally inherited leber hereditary optic neuropathy with the G14459A mutation

Mark A. Tarnopolsky, Steven K. Baker, Tomoko Myint et al. · American Journal of Medical Genetics Part A · 2003 · 76 citations

Life Sciences, Genetics, Molecular Genetics +17

Clinical, physiological, and histological features in a kindred with the T3271C MELAS mutation

Mark A. Tarnopolsky, John A. Maguire, Tomoko Myint et al. · Muscle & Nerve · 1998 · 42 citations

Life Sciences, Genetics, Molecular Genetics +17

The expanding clinical phenotype of the tRNALeu(UUR) A→G mutation at np 3243 of mitochondrial DNA: Diabetic embryopathy associated with mitochondrial cytopathy

Annette Feigenbaum, David Chitayat, Brian Robinson et al. · American Journal of Medical Genetics · 1996 · 28 citations

Life Sciences, Genetics, Molecular Genetics +17

Regulation of NADH/CoQ Oxidoreductase: Do Phosphorylation Events Affect Activity?

Mary C. Maj, Sandeep Raha, Tomoko Myint et al. · The Protein Journal · 2004 · 26 citations

Life Sciences, Biochemistry, Molecular Biology +13