Associations of α-thalassemia and BCL11A with stroke in Nigerian, United States, and United Kingdom sickle cell anemia cohorts-Reference-Cited by-同舟云学术

Associations of α-thalassemia and BCL11A with stroke in Nigerian, United States, and United Kingdom sickle cell anemia cohorts

Published:2017-04-25 Issue:11 Volume:1 Page:693-698
ISSN:2473-9529
Container-title:Blood Advances
language:en
Short-container-title:

Author:

Saraf Santosh L.¹^ORCID,Akingbola Titilola S.²,Shah Binal N.¹,Ezekekwu Chinedu A.²,Sonubi Omowunmi²,Zhang Xu¹,Hsu Lewis L.³,Gladwin Mark T.⁴⁵,Machado Roberto F.⁶,Cooper Richard S.⁷,Gordeuk Victor R.¹,Tayo Bamidele O.⁷^ORCID

Affiliation:

1. Division of Hematology and Oncology, Department of Medicine, University of Illinois at Chicago, Chicago, IL;

2. Department of Hematology, University College Hospital, Ibadan, Nigeria;

3. Division of Hematology and Oncology, Department of Pediatrics, University of Illinois at Chicago, Chicago, IL;

4. Pittsburgh Heart, Lung, Blood, and Vascular Medicine Institute and

5. Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA;

6. Division of Pulmonary and Critical Care, Department of Medicine, University of Illinois at Chicago, Chicago, IL; and

7. Department of Public Health Sciences, Stritch School of Medicine, Loyola University Chicago, Maywood, IL

Abstract

Key Points A genetic risk profile integrating α-thalassemia and BCL11A status improves associations with hemolytic markers and stroke history.

Publisher

American Society of Hematology

Subject

Hematology

Link

http://ashpublications.org/bloodadvances/article-pdf/1/11/693/877118/advances005231.pdf

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