Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng.845.pdf
Reference40 articles.
1. Albagha, O.M. et al. Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone. Nat. Genet. 42, 520–524 (2010).
2. Cooper, C. et al. The epidemiology of Paget's disease in Britain: is the prevalence decreasing? J. Bone Miner. Res. 14, 192–197 (1999).
3. Morales-Piga, A.A., Rey-Rey, J.S., Corres-Gonzalez, J., Garcia-Sagredo, J.M. & Lopez-Abente, G. Frequency and characteristics of familial aggregation of Paget's disease of bone. J. Bone Miner. Res. 10, 663–670 (1995).
4. Visconti, M.R. et al. Mutations of SQSTM1 are associated with severity and clinical outcome in Paget disease of bone. J. Bone Miner. Res. 25, 2368–2373 (2010).
5. Laurin, N., Brown, J.P., Morissette, J. & Raymond, V. Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone. Am. J. Hum. Genet. 70, 1582–1588 (2002).
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