Genome wide association study identifies variants at the CSF1, OPTN and TNFRSF11A loci as genetic risk factors for Paget¿s disease of bone
Albagha OM, Visconti MR, Alonso N, Langston AL, Cundy T, Dargie R, Dunlop MG, Fraser WD, Hooper MJ, Isaia G, Nicholson GC, del Pino Montes J, González-Sarmiento R, di Stefano M, Tenesa A, Walsh JP, Ralston SH.
Nature Genetics 42:520-524. FI: 36.377 (Q1)