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

Class:Id	LiteratureReference:5675780
_displayName	A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
_timestamp	2015-02-16 15:24:10
author	[Person:5675764] Cundy, Tim [Person:5675720] Hegde, Madhuri [Person:5675711] Naot, Dorit [Person:5675747] Chong, Belinda [Person:5675741] King, Alan [Person:5675778] Wallace, Robyn [Person:5675708] Mulley, John [Person:5675786] Love, Donald R [Person:5675737] Seidel, Joerg [Person:5675757] Fawkner, Matthew [Person:5675789] Banovic, Tatjana [Person:5675750] Callon, Karen E [Person:5675759] Grey, Andrew B [Person:5675740] Reid, Ian R [Person:5675714] Middleton-Hardie, Catherine A [Person:5675731] Cornish, Jillian
created	[InstanceEdit:5675774] Jassal, Bijay, 2015-02-16
journal	Hum. Mol. Genet.
pages	2119-27
pubMedIdentifier	12189164
title	A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
volume	11
year	2002
(literatureReference)	[Reaction:5669035] TNFSF11 binds TNFRSF11A, B [Homo sapiens]
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