A gain of function mutation in TNFRSF11B encoding osteoprotegerin causes osteoarthritis with chondrocalcinosis. [electronic resource]
- Annals of the rheumatic diseases Sep 2015
- 1756-62 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1468-2060
10.1136/annrheumdis-2013-205149 doi
Aged Aged, 80 and over Bone Resorption--genetics Cell Differentiation--genetics Chondrocalcinosis--complications Exome Female Genotype Heterozygote Humans Male Middle Aged Mutation Osteoarthritis--complications Osteoclasts Osteoprotegerin--genetics Pedigree Phenotype