Affected populations: POLG-related diseases are a group of rare, incurable conditions caused by inherited gene mutations. These disease-causing mutations are carried by up to 2% of people of ...

POLG disease is caused by inherited mutations in the POLG gene, with more than 200 known disease-causing variants. These mutations impair the enzyme responsible for maintaining mitochondrial DNA ...

PolG disease is a genetic disease caused by mutations that occur in the POLG gene in the mitochondria of a person's cell, according to the UMDF. It's one of the most commonly inherited ...

Prince Frederik, the second cousin of the heir to the Luxembourg throne, discovered at age 14 that he had a mutation in his POLG gene, which is involved in the replication and repair of DNA.

dies of rare POLG disease at 22 PolG disease is a genetic disease caused by mutations that occur in the POLG gene in the mitochondria of a person's cell, according to the UMDF. It's one of the most ...

dies of rare POLG disease at 22 PolG disease is a genetic disease caused by mutations that occur in the POLG gene in the mitochondria of a person's cell, according to the UMDF. It's one of the ...

POLG-related diseases are a group of rare, incurable conditions caused by inherited gene mutations. These disease-causing mutations are carried by up to 2% of people of Northern European descent.

POLG disease is caused by inherited mutations in the POLG gene—more than 200 disease-causing POLG mutations are known, according to the POLG Foundation. These mutations "compromise the ...

It is a serious but rare condition caused by mutations in the PolG gene. Researchers in Australia believe around one in 5000 Australian children are born with mitochondrial disease, though ...

PolG mitochondrial disease is caused by mutations in the POLG gene. It is a disorder that affects the function of mitochondria — the structures responsible for producing energy in cells.