ORMDL3 EXPRESSION IN ASM REGULATES HYPERTROPHY, HYPERPLASIA VIA TPM1 AND TPM4, AND CONTRACTILITY


Prevalence of short stature in transfusion dependent beta thalassemia patients in a tertiary care centre in North East India

crystal beaded candle holder Background: beta thalassemia is one of the most common hereditary hemoglobinopathy requiring regular blood transfusion to help reduce the complications of anemia and allow normal growth in children.Materials and Methods: It was a cross-sectional study done on 50 numbers of transfusion dependent beta thalassemia patients

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