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• W2460568082 startingPage "1512" @default.
• W2460568082 abstract "<ns4:p>Prostate cancer is a leading cause of cancer-related death in Western men. Our understanding of the genetic alterations associated with disease predisposition, development, progression, and therapy response is rapidly improving, at least in part, owing to the development of next-generation sequencing technologies. Large advances have been made in our understanding of the genetics of prostate cancer through the application of whole-exome sequencing, and this review summarises recent advances in this field and discusses how exome sequencing could be used clinically to promote personalised medicine for prostate cancer patients.</ns4:p>" @default.
• W2460568082 created "2016-07-22" @default.
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• W2460568082 date "2016-06-27" @default.
• W2460568082 modified "2023-10-04" @default.
• W2460568082 title "Advances in genetics: widening our understanding of prostate cancer" @default.
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• W2460568082 doi "https://doi.org/10.12688/f1000research.8019.1" @default.
• W2460568082 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4926757" @default.
• W2460568082 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27408704" @default.
• W2460568082 hasPublicationYear "2016" @default.
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