Ratings
0
Nobody has rated this yet. Be the first!
Works
3
FGF23 is processed by proprotein convertases but not by PHEX.
An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia.
Loss-of-function ENPP1 mutations cause both generalized arterial calcification of infancy and autosomal-recessive hypophosphatemic rickets
