A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype

Author: Love D.R.  

Publisher: Oxford University Press

E-ISSN: 0964-6906|11|18|2119-2127

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.11, Iss.18, 2002-06, pp. : 2119-2127

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