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Hematology Volume 22, 2017 - Issue 6
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Enzymopathy

Possible association of 3′ UTR +357 A>G, IVS11-nt 93 T>C, c.1311 C>T polymorphism with G6PD deficiency

Mahmoud M. SirdahBiology Department, Al Azhar University-Gaza, Gaza, Palestine;Division of Hematology, Department of Internal Medicine, School of Medicine, University of Utah, Salt Lake City, UT, USACorrespondence[email protected]
[email protected]
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,
Mohammad E. ShubairDepartment of Medical Laboratory Sciences, Islamic University-Gaza, Gaza, PalestineView further author information
,
Mustafa S. Al-KahloutPalestinian Ministry of Health, Al Nasser Pediatric Hospital, PalestineView further author information
,
Jamal M. Al-TayebPalestinian Ministry of Health, Al Nasser Pediatric Hospital, PalestineView further author information
,
Josef T. PrchalDivision of Hematology, Department of Internal Medicine, School of Medicine, University of Utah, Salt Lake City, UT, USA;Institute for Clinical and Experimental Pathology, ARUP Laboratories, Salt Lake City, UT, USAView further author information
&
N. Scott ReadingDivision of Hematology, Department of Internal Medicine, School of Medicine, University of Utah, Salt Lake City, UT, USA;Institute for Clinical and Experimental Pathology, ARUP Laboratories, Salt Lake City, UT, USACorrespondence[email protected]
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Pages 370-374 | Published online: 06 Jan 2017

References

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  • Reading NS, Sirdah MM, Shubair ME, et al. Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community. Blood Cell Mol Dis. 2016;60:58–64.
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