Significats de congenital insensitivity en anglès

PRDM12 is the third human gene to be associated with congenital insensitivity to pain.

Now, Woods and his colleagues have discovered yet more mutations that cause congenital insensitivity to pain.

Curry cure | Mo Costandi Read more Ashlyn is one of a tiny number of people with congenital insensitivity to pain.

Nav1.7 is a genetically validated pain target in humans, as loss-of-function mutations cause congenital insensitivity to pain, and gain-of-function mutations cause severe pain syndromes.