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Leigh Syndrome mtDNA mutation
Did you mean light Syndrome mtDNA mutation?
- ... Genetic Testing Registry: Leigh syndrome Genetic Testing Registry: Leigh Syndrome (mtDNA mutation) Genetic Testing Registry: Leigh Syndrome (nuclear DNA mutation) ...
- ... common than a similar but more severe condition, Leigh syndrome, which affects about 1 in 40,000 people. NARP results from mutations in the MT-ATP6 gene. This gene is contained in mitochondrial DNA, also known as mtDNA. Mitochondria are structures within cells that convert the ...
- ... developing embryo, children can inherit disorders resulting from mtDNA mutations only from their mother. These disorders can appear in every generation of a family and can affect both males and females, but fathers do not pass traits associated with changes in mtDNA to their ... synthase deficiency Genetic Testing ...
- ... developing embryo, children can inherit disorders resulting from mtDNA mutations only from their mother. These disorders can appear in every generation of a family and can affect both males and females, but fathers do not pass traits ... NADH-coenzyme Q reductase deficiency ...
- ... embryo, children can only inherit disorders resulting from mtDNA mutations from their mother. These disorders can appear in every generation of a family and can affect both males and females, but fathers do not pass traits ... Complex IV deficiency COX deficiency ...
- ... Islands in the North Atlantic Ocean. SUCLA2-related mtDNA depletion syndrome is caused by variants (also called mutations) in the SUCLA2 gene. The SUCLA2 gene provides ...
