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Mutation Spectrum of β-Globin Gene in Patients with β-Thalassemia at Tidar Hospital, Magelang, Central Java, Indonesia.

Hemoglobin - 1 Nov 2023

'Ulya Nafis Muhimmatul, Indrawati Vera Nurohmah, Wulansari Woro Triaksiwi, Lesmana Indra, Handayani Niken Satuti Nur

Abstract excerpt

β-Thalassemia is genetic disorder characterized by β-globin chain deficiency resulting from mutations in the β-globin coding gene. Both the quantity and quality of blood produced will be impacted by this condition. The distribution of mutation causing thalassemia is vary across ethnic and different regions in Indonesia. This study aims to identify the variant mutation in patients with β-thalassemia at Tidar...

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PMID: 37605561
DOI: 10.1080/03630269.2023.2244429

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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