People with leigh syndrome. Medical search. Frequent questions

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Anatomy3

Mitochondria Fibroblasts Brain

Diseases10

Leigh Disease Cytochrome-c Oxidase Deficiency Syndrome Brain Diseases, Metabolic Mitochondrial Encephalomyopathies Mitochondrial Diseases MELAS Syndrome Encephalomalacia Down Syndrome Metabolic Syndrome X

Chemicals and Drugs8

Electron Transport Complex I Mitochondrial Proteins NADH Dehydrogenase Mitochondrial Proton-Translocating ATPases Electron Transport Complex IV DNA, Mitochondrial Membrane Proteins Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment3

DNA Mutational Analysis Pedigree Magnetic Resonance Imaging

Phenomena and Processes3

Mutation Oxidative Phosphorylation Founder Effect

Information Science1

Molecular Sequence Data

Named Groups1

Infant, Newborn

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Information Science Named Groups

Leigh Disease Cytochrome-c Oxidase Deficiency Syndrome Electron Transport Complex I Brain Diseases, Metabolic Mitochondrial Encephalomyopathies Mitochondrial Proteins Mitochondrial Diseases NADH Dehydrogenase Mitochondrial Proton-Translocating ATPases Electron Transport Complex IV DNA, Mitochondrial MELAS Syndrome Mutation Encephalomalacia Oxidative Phosphorylation Mitochondria Founder Effect Membrane Proteins DNA Mutational Analysis Pedigree Fibroblasts Brain Down Syndrome Metabolic Syndrome X Proteins Infant, Newborn Magnetic Resonance Imaging Molecular Sequence Data

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