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 Latest Science News -- ScienceDaily https://ift.tt/2RCAPpq
at
Labels:

No comments:

Post a Comment

Subscribe to: Post Comments (Atom)

Stanford scientists discover the human brain may actually be two separate organs

Scientists have found that the human brain develops from two distinct cellular systems, suggesting that evolution fused together two ancient...