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Article

Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India

1 Jan 2010

Abstract excerpt

BACKGROUND: Sickle cell-β thalassemia (HbS-β thalassemia) is a sickling disorder of varying severity, which results from compound heterozygosity for sickle cell trait and β thalassemia trait. The present study was undertaken to determine the genetic factors responsible for the clinical variability of HbS-β thalassemia patients from western India. MATERIALS AND METHODS: Twenty-one HbS-β thalassemia cases with...

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PMID: 21206704
DOI: 10.4103/0971-6866.73410

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