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Tags: 2007, AIM, Backlog, Cause Of Death, Chevalier I, Child, Cohort Studies, Debray FG, Decarie JC, DNA, DNA Fragmentation, Female, Follow-up Studies, HEREDITARY, Humans, IM, Infant, Journal Article, Lambert M, Leber/di [Diagnosis], Leber/ge [Genetics], Leber/mo [Mortality], Longitudinal Studies, Male, MELAS Syndrome/di [Diagnosis], MELAS Syndrome/mo [Mortality], MELAS Syndrome/th [Therapy], Mitchell GA, Mitochondrial Diseases/di [Diagnosis], Mitochondrial Diseases/ge [Genetics], Mitochondrial Diseases/mo [Mortality], Mitochondrial Encephalomyopathies/di [Diagnosis], Mitochondrial Encephalomyopathies/mo [Mortality], Mitochondrial Encephalomyopathies/th [therapy], Mitochondrial Myopathies/di [Diagnosis], Mitochondrial Myopathies/ge [Genetics], Mitochondrial Myopathies/mo [Mortality], Mitochondrial/ge [Genetics], Newborn, Optic Atrophy, Pediatrics, Preschool, Probability, Proportional Hazards Models, Q3 Scoping Review Results, Retrospective Studies, Robinson BH, Robitaille Y, Severity Of Illness Index, Shoubridge EA, Survival Analysis, Time Factors
Tags: 2001, American Journal Of Human Genetics, Backlog, Base Sequence, Chromosome Mapping, Chromosomes, Cytochrome-c Oxidase Deficiency, Daly MJ, Delmonte T, Disease Specific, DNA Mutational Analysis, DNA/chemistry/genetics, Electron Transport Complex IV/genetics, Family Health, Female, Gene Frequency, Genes/genetics, Genome, Haplotypes, Hudson TJ, Human, Humans, Journal Article, Lander ES, Lee N, Leigh Disease/enzymology/genetics, Linkage Disequilibrium, Male, Microsatellite Repeats, Mitchell GA, Molecular Sequence Data, Morin CC, Mutation, Pair 2/genetics, Pedigree, Polymorphism, Rioux JD, Robinson BH, Single Nucleotide, Xu F