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GTR Home > Tests > Comprehensive Mitochondrial Mutation Detection

Indication

This is a clinical test intended for Help: Diagnosis, Mutation Confirmation, Pre-symptomatic, Risk Assessment, Screening

Clinical summary

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Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. [from MeSH]

Conditions tested

Target population

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General population with clinical diagnosis of disease

Citations

Not provided

Clinical validity

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Not provided

Clinical utility

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Not provided

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