Sickle cell anemia and α-thalassemia: A modulating factor in homozygous HbS/S patients in Oman.

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Bibliographic Details
Title: Sickle cell anemia and α-thalassemia: A modulating factor in homozygous HbS/S patients in Oman.
Authors: Hassan, S.M.1,2 suha_85@hotmail.com, Al Muslahi, M.3, Al Riyami, M.3, Bakker, E.2, Harteveld, C.L.2, Giordano, P.C.2
Source: European Journal of Medical Genetics. Nov2014, Vol. 57 Issue 11/12, p603-606. 4p.
Database: Academic Search Ultimate
Description
ISSN:17697212
DOI:10.1016/j.ejmg.2014.09.005