Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene

Hodgkin lymphoma shows strong familial aggregation but no major susceptibility genes have been identified to date. The goal of this study was to identify high-penetrance variants using whole exome sequencing in 17 Hodgkin lymphoma prone families with three or more affected cases or obligate carriers...

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Detaylı Bibliyografya
Yayımlandı:Haematologica
Asıl Yazarlar: Rotunno, Melissa, McMaster, Mary L., Boland, Joseph, Bass, Sara, Zhang, Xijun, Burdett, Laurie, Hicks, Belynda, Ravichandran, Sarangan, Luke, Brian T., Yeager, Meredith, Fontaine, Laura, Hyland, Paula L., Goldstein, Alisa M., Chanock, Stephen J., Caporaso, Neil E., Tucker, Margaret A., Goldin, Lynn R.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Ferrata Storti Foundation 2016
Konular:
Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5004465/
https://ncbi.nlm.nih.gov/pubmed/27365461
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2015.135475
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