Genome-wide Copy-Number-Variation Study Identified a Susceptibility Gene, UGT2B17, for Osteoporosis

Osteoporosis, a highly heritable disease, is characterized mainly by low bone-mineral density (BMD), poor bone geometry, and/or osteoporotic fractures (OF). Copy-number variation (CNV) has been shown to be associated with complex human diseases. The contribution of CNV to osteoporosis has not been d...

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Main Authors: Yang, Tie-Lin, Chen, Xiang-Ding, Guo, Yan, Lei, Shu-Feng, Wang, Jin-Tang, Zhou, Qi, Pan, Feng, Chen, Yuan, Zhang, Zhi-Xin, Dong, Shan-Shan, Xu, Xiang-Hong, Yan, Han, Liu, Xiaogang, Qiu, Chuan, Zhu, Xue-Zhen, Chen, Teng, Li, Meng, Zhang, Hong, Zhang, Liang, Drees, Betty M., Hamilton, James J., Papasian, Christopher J., Recker, Robert R., Song, Xiao-Ping, Cheng, Jing, Deng, Hong-Wen
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2667994/
https://ncbi.nlm.nih.gov/pubmed/18992858
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2008.10.006
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