<i>In silico</i>
            analysis of substitution mutations in the β-globin gene in Turkish population of β-thalassemia

Alkilani, Sima; Sevimoglu, Tuba

doi:10.1080/07391102.2023.2176924

Cited by 1 publication

(1 citation statement)

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“…18 Each individual with thalassemia major carried an abnormal beta globin protein. 19 With passage of time HBB blockage leads to decrease beta-chain synthesis and body failed to build up new beta-chains leads to under production of adult hemoglobin. 20 Every year 60,000 infants are born with beta thalassemia major.…”

Section: Introductionmentioning

confidence: 99%

Frequency Of Beta Thalassemia Major Abo Blood Groups In Different Foundation Of District Peshawar

Imran Khan,

Rabnawaz,

Ullah

et al. 2024

NJLHS

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Background: Thalassemia major (TM) is an inherited hemolytic disorder occur due to abnormal hemoglobin production as a result of HBB (Haemoglobin Subunit Beta) gene mutation because HBB gene provides instructions for making of beta globin. The research study aim is to determine the frequency of beta thalassemia major ABO blood group in different foundation of district Peshawar. Methods: A descriptive cross-sectional study was conducted, involving 100 individuals with Thalassemia major from different foundations in Peshawar, including Hamza Foundation and Fatmid Foundation. The data was analyzed for statistical analysis using SPSS version 22.0 software. Results: The study analyzed the gender-wise distribution of Thalassemia major patients, revealing that out of the 100 individuals, 43 were female (43%) and 57 were male (57%). Moreover, the study examined the ABO blood types among the participants. The most prevalent blood type among the Thalassemia major patients was B+ (35.0%), followed by O+ (34.0%), A+ (26.0%), AB+ (4.0%), and O- (1.0%). Conclusion: Based on the results, it can be said that among those with Thalassemia major in the population under study, the B+ blood type is the most prevalent and well-known ABO blood group.

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Section: Introductionmentioning

confidence: 99%