A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
Open Access
- 1 September 2002
- journal article
- research article
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 11 (18), 2119-2127
- https://doi.org/10.1093/hmg/11.18.2119