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

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Published in Hum Mol Genet on September 01, 2002

Authors

Tim Cundy1, Madhuri Hegde, Dorit Naot, Belinda Chong, Alan King, Robyn Wallace, John Mulley, Donald R Love, Joerg Seidel, Matthew Fawkner, Tatjana Banovic, Karen E Callon, Andrew B Grey, Ian R Reid, Catherine A Middleton-Hardie, Jillian Cornish

Author Affiliations

1: Department of Medicine, Faculty of Medicine and Health Science, University of Auckland, New Zealand. t.cundy@auckland.ac.nz

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