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

Chang, BL (author)
Cramer, SD (author)
Wiklund, F (author)
Karolinska Institutet
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Isaacs, SD (author)
Stevens, VL (author)
Sun, J (author)
Smith, S (author)
Pruett, K (author)
Romero, LM (author)
Wiley, KE (author)
Kim, ST (author)
Zhu, Y (author)
Zhang, Z (author)
Hsu, FC (author)
Turner, AR (author)
Adolfsson, J (author)
Karolinska Institutet
Liu, W (author)
Kim, JW (author)
Duggan, D (author)
Carpten, J (author)
Zheng, SL (author)
Rodriguez, C (author)
Isaacs, WB (author)
Gronberg, H (author)
Karolinska Institutet
Xu, JF (author)
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 (creator_code:org_t)
2009-01-08
2009
English.
In: Human molecular genetics. - : Oxford University Press (OUP). - 1460-2083 .- 0964-6906. ; 18:7, s. 1368-1375
  • Journal article (peer-reviewed)
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