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 Top Health News -- ScienceDaily https://ift.tt/2RCAPpq
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Study finds untreated sleep apnea doubles Parkinson’s risk

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