Complex i deficiency. Medical search. Frequent questions

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Anatomy8

Mitochondria Fibroblasts Mitochondria, Muscle Cell Nucleus Cells, Cultured Mitochondria, Heart Skin Submitochondrial Particles

Organisms2

Yarrowia Mice, Knockout

Diseases22

Leigh Disease Mitochondrial Diseases Mitochondrial Encephalomyopathies MELAS Syndrome Metabolism, Inborn Errors Mitochondrial Myopathies Hyperargininemia Carbamoyl-Phosphate Synthase I Deficiency Disease Protein C Deficiency Protein S Deficiency Vitamin A Deficiency Deficiency Diseases alpha 1-Antitrypsin Deficiency Vitamin B 12 Deficiency Vitamin D Deficiency Folic Acid Deficiency IgA Deficiency Thiamine Deficiency Glucosephosphate Dehydrogenase Deficiency Magnesium Deficiency Vitamin E Deficiency Ascorbic Acid Deficiency

Chemicals and Drugs21

Electron Transport Complex I NADH Dehydrogenase NAD(P)H Dehydrogenase (Quinone)DNA, Mitochondrial Rotenone NADH, NADPH Oxidoreductases Mitochondrial Proteins Complement Factor I Ubiquinone Electron Transport Complex II Quinone Reductases Electron Transport Complex III Protein Subunits Uncoupling Agents Electron Transport Chain Complex Proteins Proton Pumps Secosteroids Reactive Oxygen Species Iron-Sulfur Proteins Succinic Acid Interleukin-11 Receptor alpha Subunit

Analytical, Diagnostic and Therapeutic Techniques and Equipment3

DNA Mutational Analysis Fatal Outcome Pedigree

Phenomena and Processes13

Oxidative Phosphorylation Mutation Phenotype Consanguinity Homozygote Electron Transport Point Mutation Heterozygote Base Sequence Amino Acid Sequence Cell Respiration Oxidation-Reduction Oxygen Consumption

Information Science4

Fatal Outcome Molecular Sequence Data Base Sequence Amino Acid Sequence

Named Groups1

Infant, Newborn

Health Care1

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

Electron Transport Complex I Leigh Disease Mitochondrial Diseases NADH Dehydrogenase NAD(P)H Dehydrogenase (Quinone)Mitochondrial Encephalomyopathies MELAS Syndrome Mitochondria DNA, Mitochondrial Metabolism, Inborn Errors Oxidative Phosphorylation Rotenone Mitochondrial Myopathies NADH, NADPH Oxidoreductases Fibroblasts Hyperargininemia Mitochondria, Muscle Mutation Mitochondrial Proteins Complement Factor I DNA Mutational Analysis Fatal Outcome Pedigree Carbamoyl-Phosphate Synthase I Deficiency Disease Infant, Newborn Cell Nucleus Phenotype Protein C Deficiency Yarrowia Cells, Cultured Consanguinity Homozygote Protein S Deficiency Molecular Sequence Data Mitochondria, Heart Electron Transport Ubiquinone Electron Transport Complex II Point Mutation Vitamin A Deficiency Quinone Reductases Deficiency Diseases Heterozygote Electron Transport Complex III Base Sequence Skin alpha 1-Antitrypsin Deficiency Amino Acid Sequence Vitamin B 12 Deficiency Protein Subunits Vitamin D Deficiency Cell Respiration Uncoupling Agents Folic Acid Deficiency Electron Transport Chain Complex Proteins IgA Deficiency Proton Pumps Thiamine Deficiency Submitochondrial Particles Secosteroids Reactive Oxygen Species Oxidation-Reduction Glucosephosphate Dehydrogenase Deficiency Mice, Knockout Iron-Sulfur Proteins Succinic Acid Magnesium Deficiency Interleukin-11 Receptor alpha Subunit Vitamin E Deficiency Ascorbic Acid Deficiency Oxygen Consumption

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