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Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms
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Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone
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Founder effect in different European countries for the recurrent P392L SQSTM1 mutation in Paget's disease of bone
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Identification of sex-specific associations between. polymorphisms of the Osteoprotegerin gene, TNFRSF11B, and Paget's disease of bone