Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 7, p. 1368, doi. 10.1093/hmg/ddp035

By:

• Chang, Bao-Li;
• Cramer, Scott D.;
• Wiklund, Fredrik;
• Isaacs, Sarah D.;
• Stevens, Victoria L.;
• Sun, Jielin;
• Smith, Shelly;
• Pruett, Kristen;
• Romero, Lina M.;
• Wiley, Kathleen E.;
• Kim, Seong-Tae;
• Zhu, Yi;
• Zhang, Zheng;
• Hsu, Fang-Chi;
• Turner, Aubrey R.;
• Adolfsson, Jan;
• Liu, Wennuan;
• Kim, Jin Woo;
• Duggan, David;
• Carpten, John

Publication type:

Article