Coinheritance of sickle cell anemia and α-thalassemia delays disease onset and could improve survival in Cameroonian's patients (Sub-Saharan Africa).

Am J Hematol

Division of Human Genetics, Institute of Infectious Disease and Molecular Medicine (IDM), Faculty of Health Sciences, University of Cape Town (UCT), Cape Town, Republic of South Africa.

Published: June 2014

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.23711DOI Listing

Publication Analysis

Top Keywords

coinheritance sickle
4
sickle cell
4
cell anemia
4
anemia α-thalassemia
4
α-thalassemia delays
4
delays disease
4
disease onset
4
onset improve
4
improve survival
4
survival cameroonian's
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!