Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

Mitochondrial mutation

Mitochondrial mutations are mutations of DNA that is encapsulated in mitochondria. Those mutations exhibit a wide variability in frequency among cell of an organisms individuals of the same family (heteroplasmy). Inheritance is maternal.

Related terms:

mutation heteroplasmy homoplasmy
Copyright © 2005-2021 by Center for Nephrology and Metabolic Disorders, Dr. Mato Nagel, MD
Albert-Schweitzer-Ring 32, D-02943 Weißwasser, Germany, Tel.: +49-3576-287922, Fax: +49-3576-287944
Sitemap | Webmail | Disclaimer | Privacy Issues | Website Credits