Chang, Bao-Li <br/><br/>
Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk.  [electronic resource] 

 -  Human molecular genetics  Apr 2009 
 - 1368-75 p.  digital 
<br/><br/> 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. 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddp035  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Androgens--pharmacology<br/>Base Sequence<br/>Chromosomes, Human, Pair 10--genetics<br/>Genetic Predisposition to Disease<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Physical Chromosome Mapping<br/>Polymorphism, Single Nucleotide--genetics<br/>Promoter Regions, Genetic--genetics<br/>Prostatic Neoplasms--genetics<br/>Prostatic Secretory Proteins--genetics<br/>Sweden