The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival. [electronic resource]
Producer: 20150219Description: e100516 p. digitalISSN:- 1932-6203
- Adolescent
- Adult
- Age Factors
- Anemia, Sickle Cell -- blood
- Blood Cell Count
- Cameroon
- Female
- Gene Deletion
- Haplotypes
- Hemoglobin A -- genetics
- Hemoglobin, Sickle -- genetics
- Humans
- Inheritance Patterns
- Male
- Multigene Family
- Polymorphism, Single Nucleotide
- Referral and Consultation -- statistics & numerical data
- Survival Analysis
- alpha-Globins -- genetics
- alpha-Thalassemia -- blood
- beta-Globins -- genetics
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Publication Type: Journal Article
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