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Publications by John W. Yarham
Pathogenic Mitochondrial tRNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease
Human Mutation
Genetics
Related publications
Novel and Heteroplasmic Mutations in Mitochondrial tRNA Genes in Brugada Syndrome
Cardiology Journal
Medicine
Cardiovascular Medicine
Cardiology
Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis
American Journal of Human Genetics
Genetics
Mutations in the Mitochondrial Tryptophanyl‐tRNA Synthetase Cause Growth Retardation and Progressive Leukoencephalopathy
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Exome Sequencing Identifies Mitochondrial Alanyl-tRNA Synthetase Mutations in Infantile Mitochondrial Cardiomyopathy
American Journal of Human Genetics
Genetics
Mitochondrial Mutations
Genome Biology
Novel Point Mutations in Mitochondrial 16S rRNA Gene of Chinese Hamster Cells.
Genes and Genetic Systems
Medicine
Genetics
Molecular Biology
Mutations in Mitochondrial Histidyl tRNA Synthetase HARS2 Cause Ovarian Dysgenesis and Sensorineural Hearing Loss of Perrault Syndrome
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Two Pathogenic Point Mutations Exist in the Authentic Mitochondrial Genome, Not in the Nuclear Pseudogene
Journal of Human Genetics
Genetics
The Impact of Pathogenic Mitochondrial DNA Mutations on Substantia Nigra Neurons
Journal of Neuroscience
Neuroscience