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Publications by M Chol
The Mitochondrial DNA G13513A MELAS Mutation in the NADH Dehydrogenase 5 Gene Is a Frequent Cause of Leigh-Like Syndrome With Isolated Complex I Deficiency
Journal of Medical Genetics
Genetics
Related publications
NDUFB8 Mutations Cause Mitochondrial Complex I Deficiency in Individuals With Leigh-Like Encephalomyopathy
American Journal of Human Genetics
Genetics
Mitochondrial DNA-associated Leigh Syndrome
Inhibitory Effects of Tannins on the NADH Dehydrogenase Activity of Bovine Heart Mitochondrial Complex I.
Biological and Pharmaceutical Bulletin
Medicine
Pharmacology
Pharmaceutical Science
Overlapping Leigh Syndrome/Myoclonic Epilepsy With Ragged Red Fibres in an Adolescent Patient With a Mitochondrial DNA A8344G Mutation
Frontiers in Neurology
Neurology
The Prevalence of Mitochondrial DNA Mutations in Leigh Syndrome in a Brazilian Series
Medical Express
MERRF/MELAS Overlap Syndrome: A Double Pathogenic Mutation in Mitochondrial tRNA Genes
Journal of Medical Genetics
Genetics
Nonneutral Evolution at the Mitochondrial NADH Dehydrogenase Subunit 3 Gene in Mice.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Mutation in the E1α Subunit of Pyruvate Dehydrogenase Associated With Variable Expression of Pyruvate Dehydrogenase Complex Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Succination Is Increased on Select Proteins in the Brainstem of the NADH Dehydrogenase (Ubiquinone) Fe-S Protein 4 (Ndufs4) Knockout Mouse, a Model of Leigh Syndrome
Molecular and Cellular Proteomics
Biochemistry
Medicine
Analytical Chemistry
Molecular Biology
