Article

Detection of Common Deletion Mutations (− α<sup>3.7</sup>and − α<sup>4.2</sup>kb) in<i>HBA</i>gene and Genotype-Phenotype Correlation

2024-09-04

Abstract excerpt

<h4>ABSTRACT</h4> <h4>Background and Objectives</h4> Microcytic hypochromic anemia is the most common feature of alpha-thalassemia and depends on the number of alpha genes deleted. Therefore, in this study, we aim to determine the most common deletion mutations among microcytic anemia cases of West Bengal and correlate them with different biochemical parameters and endophenotypes. <h4>Methods</h4> Two hundred and...

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Literature Corpus work: a8c039dd-79dd-54d5-8484-098c548f341c
DOI: 10.1101/2024.09.03.24312976

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Detection of Common Deletion Mutations (− α<sup>3.7</sup>and − α<sup>4.2</sup>kb) in<i>HBA</i>gene and Genotype-Phenotype CorrelationDOI 10.1101/2024.09.03.24312976Read

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