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Am J Hematol. 2014 Jun;89(6):664-5. doi: 10.1002/ajh.23711. Epub 2014 Apr 10.

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

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1
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.
PMID:
24639123
DOI:
10.1002/ajh.23711
[Indexed for MEDLINE]
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