Hemoglobin
Identification of Sickle Cell Disease and Its Associated Other Structural Variants of Hemoglobin Using High Performance Liquid Chromatography and Their Clinical Profiling.
Dhirendra Kumar, Lokeswara Bala Krishna S, Sridevi Parikipandla
Published: 202610.1080/03630269.2025.2590259
Abstract
Sickle cell disease (SCD), a well known hemoglobinopathy, is a recessive inherited blood abnormality caused by point mutation in hemoglobin proteins, notably prevalent in the tribal belt of Madhya Pradesh, India. The study aims to identify the SCD-as…
Preview only. Read the full abstract at the source