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Genetic Modifiers of Sickle Cell Disease
Sickle cell anemia is associated with unusual clinical heterogeneity for a Mendelian disorder. Fetal hemoglobin concentration and coincident ∝ thalassemia, both which directly affect the sickle erythrocyte, are the major modulators of the phenotype of disease. Understanding the genetics underlying t...
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| Yayımlandı: | Am J Hematol |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4562292/ https://ncbi.nlm.nih.gov/pubmed/22641398 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajh.23232 |
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