Genomic architecture of sickle cell disease in West African children

Sickle cell disease (SCD) is a congenital blood disease, affecting predominantly children from sub-Saharan Africa, but also populations world-wide. Although the causal mutation of SCD is known, the sources of clinical variability of SCD remain poorly understood, with only a few highly heritable trai...

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Detaylı Bibliyografya
Asıl Yazarlar: Quinlan, Jacklyn, Idaghdour, Youssef, Goulet, Jean-Philippe, Gbeha, Elias, de Malliard, Thibault, Bruat, Vanessa, Grenier, Jean-Christophe, Gomez, Selma, Sanni, Ambaliou, Rahimy, Mohamed C., Awadalla, Philip
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2014
Konular:
Genetics
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3924578/
https://ncbi.nlm.nih.gov/pubmed/24592274
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2014.00026
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