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Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH.
Williams CJ, Zhang Y, Timms A, Bonavita G, Caeiro F, Broxholme J, Cuthbertson J, Jones Y, Marchegiani R, Reginato A, Russell RG, Wordsworth BP, Carr AJ, Brown MA. Williams CJ, et al. Among authors: zhang y. Am J Hum Genet. 2002 Oct;71(4):985-91. doi: 10.1086/343053. Epub 2002 Sep 17. Am J Hum Genet. 2002. PMID: 12297989 Free PMC article.
Genetic studies of chondrocalcinosis.
Zhang Y, Brown MA. Zhang Y, et al. Curr Opin Rheumatol. 2005 May;17(3):330-5. doi: 10.1097/01.bor.0000157042.19740.f4. Curr Opin Rheumatol. 2005. PMID: 15838246 Review.
Influence of LRP5 polymorphisms on normal variation in BMD.
Koay MA, Woon PY, Zhang Y, Miles LJ, Duncan EL, Ralston SH, Compston JE, Cooper C, Keen R, Langdahl BL, MacLelland A, O'Riordan J, Pols HA, Reid DM, Uitterlinden AG, Wass JA, Brown MA. Koay MA, et al. Among authors: zhang y. J Bone Miner Res. 2004 Oct;19(10):1619-27. doi: 10.1359/JBMR.040704. Epub 2004 Jul 7. J Bone Miner Res. 2004. PMID: 15355556 Free article.
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