Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk. [electronic resource]
Producer: 20090518Description: 1368-75 p. digitalISSN:- 1460-2083
- Androgens -- pharmacology
- Base Sequence
- Chromosomes, Human, Pair 10 -- genetics
- Genetic Predisposition to Disease
- Humans
- Male
- Molecular Sequence Data
- Physical Chromosome Mapping
- Polymorphism, Single Nucleotide -- genetics
- Promoter Regions, Genetic -- genetics
- Prostatic Neoplasms -- genetics
- Prostatic Secretory Proteins -- genetics
- Sweden
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
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