ENIGMA - Evidence-based Network for the Interpretation of Germline Mutant Alleles: An international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes

As genetic testing for predisposition to human diseases has become an increasingly common practice in medicine, the need for clear interpretation of the test results is apparent. However, for many disease genes, including the breast cancer susceptibility genes BRCA1 and BRCA2, a significant fraction...

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Bibliografiset tiedot
Päätekijät: Spurdle, Amanda B, Healey, Sue, Devereau, Andrew, Hogervorst, Frans BL, Monteiro, Alvaro NA, Nathanson, Katherine L, Radice, Paolo, Stoppa-Lyonnet, Dominique, Tavtigian, Sean, Wappenschmidt, Barbara, Couch, Fergus J, Goldgar, David E
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2011
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3240687/
https://ncbi.nlm.nih.gov/pubmed/21990146
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.21628
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