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Association between a variation in the phosphodiesterase 4D gene and bone mineral density
Authors:Richard?H?Reneland,Steven?Mah,Stefan?Kammerer,Carolyn?R?Hoyal,George?Marnellos,Scott?G?Wilson,Philip?N?Sambrook,Tim?D?Spector,Matthew?R?Nelson,Andreas?Braun  author-information"  >  author-information__contact u-icon-before"  >  mailto:abraun@sequenom.com"   title="  abraun@sequenom.com"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Sequenom, Inc., San Diego, California, USA;(2) Department of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Perth, Australia;(3) Rheumatology Unit, Royal North Shore Hospital, NSW, Australia;(4) Twin Research & Genetic Epidemiology Unit, St Thomas Hospital, London, UK
Abstract:

Background  

Fragility fractures caused by osteoporosis are a major cause of morbidity and mortality in aging populations. Bone mineral density (BMD) is a useful surrogate marker for risk of fracture and is a highly heritable trait. The genetic variants underlying this genetic contribution are largely unknown.
Keywords:
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