Inheritance of rare functional GCKR variants and their contribution to triglyceride levels in families

Significant resources have been invested in sequencing studies to investigate the role of rare variants in complex disease etiology. However, the diagnostic interpretation of individual rare variants remains a major challenge, and may require accurate variant functional classification and the collec...

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Detaylı Bibliyografya
Asıl Yazarlar: Rees, Matthew G., Raimondo, Anne, Wang, Jian, Ban, Matthew R., Davis, Mindy I., Barrett, Amy, Ranft, Jessica, Jagdhuhn, David, Waterstradt, Rica, Baltrusch, Simone, Simeonov, Anton, Collins, Francis S., Hegele, Robert A., Gloyn, Anna L.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2014
Konular:
Association Studies Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4168830/
https://ncbi.nlm.nih.gov/pubmed/24879641
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu269
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