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Article

An initiation codon mutation as a cause of a beta-thalassemia.

Hemoglobin - 1 Jan 1990

Jankovic L, Efremov G D, Josifovska O, Juricic D, Stoming T A, Kutlar A, Huisman T H

Abstract excerpt

During the course of a screening program for beta-thalassemia mutations among beta-thalassemia heterozygotes in Yugoslavia we observed a mutation (ATG----ACG) in the initiation codon of the beta-globin gene which has not been described before. The abnormality was initially detected through mapping of the beta-globin gene by Southern blot analysis using the restriction enzyme Nco I. The loss of the Nco I site...

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Identifiers

PMID: 2272840
DOI: 10.3109/03630269009046958

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CAT

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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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