Perspective: A novel prognostic for sickle cell disease

Sickle hemoglobin (α2βS2) polymerization drives disease pathophysiology in sickle cell anemia. Fetal hemoglobin (α2γ2) restricts disease severity by inhibiting the polymerization of sickle hemoglobin in a concentration-dependent manner. Clinical decision-making relies on diagnostic technologies eval...

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Bibliographic Details
Main Authors: Brian M Mozeleski, Abdullah Al-Rubaish, Amein Al-Ali, Jose Romero
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Saudi Journal of Medicine and Medical Sciences
Subjects:
Online Access:http://www.sjmms.net/article.asp?issn=1658-631X;year=2018;volume=6;issue=3;spage=133;epage=136;aulast=Mozeleski