Wednesday, January 29, 2020

Disease-aggravating mutation found in a mouse model of neonatal mitochondrial disease

The new mitochondrial DNA (mtDNA) variant drastically speeds up the disease progression in a mouse model of GRACILE syndrome. This discovery provides a new tool for studies of mitochondrial diseases.

from Health & Medicine News -- ScienceDaily https://www.sciencedaily.com/releases/2020/01/200129104709.htm

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