Coinheritance of α-Thalassemia Decreases the Risk of Cerebrovascular Disease in a Cohort of Children with Sickle Cell Anemia-Reference-Cited by-同舟云学术

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Coinheritance of α-Thalassemia Decreases the Risk of Cerebrovascular Disease in a Cohort of Children with Sickle Cell Anemia

Published:2010-11-15 Issue:6 Volume:34 Page:516-529
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Belisário André Rolim,Rodrigues Cibele Velloso,Martins Marina Lobato,Silva Célia Maria,Viana Marcos Borato

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2010.526003

Reference52 articles.

1. Genetic Modifiers in Hemoglobinopathies

2. Predicting clinical severity in sickle cell anaemia

3. EFFECT OF α-GLOBIN GENOTYPE ON THE PATHOPHYSIOLOGY OF SICKLE CELL DISEASE

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