A study conducted by researchers at IRCCS Ospedale San Raffaele Milano, funded by Telethon and coordinated by Prof. Sonia Levi was published in The Journal of Experimental Medicine.
Monthly Archives: September 2013
Mitochondrial diseases: here’s the metabolism-helper gene
A case of malfunctioning mitochondria? Considerable help may be provided by OPA1 – a gene which, when altered, is known to be responsible for a hereditary disease of the eye, dominant optic atrophy.