Ralston, Stuart H.Uitterlinden, André G.Brandi, Maria LuisaBalcells Comas, SusanaLangdahl, Bente L.Lips, PaulLorenc, RomanObermayer-Pietsch, BarbaraScollen, SerenaBustamante Pineda, MarionaBjerre Husted, LiseCarey, Alisoun H.Díez Pérez, AdolfoDunning, Alison M.Falchetti, AlbertoKarczmarewicz, ElzbietaKruk, Marcin2013-05-082013-05-082006-041549-1277https://hdl.handle.net/2445/43234Osteoporosis and fracture risk are considered to be under genetic control. Extensive work is being performed to identify the exact genetic variants that determine this risk. Previous work has suggested that a G/T polymorphism affecting an Sp1 binding site in the COLIA1 gene is a genetic marker for low bone mineral density (BMD) and osteoporotic fracture, but there have been no very-large-scale studies of COLIA1 alleles in relation to these phenotypes.9 p.application/pdfengcc-by (c) Ralston, S.H. et al., 2006http://creativecommons.org/licenses/by/3.0/esOsteoporosiGenòmicaDensitometria òssiaOsteoporosisGenomicsBone densitometryinfo:eu-repo/semantics/article5453362013-05-08info:eu-repo/semantics/openAccess