Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene

Hemoglobin. 1990;14(2):157-68. doi: 10.3109/03630269009046957.

Abstract

DNA analysis of a Northern Thai family with a child affected with beta-thalassemia major revealed a novel deletion of 3.4 kb removing the entire beta-globin gene in the proposita and her mother. Detailed mapping of the deletion located the 5' breakpoint in the region between nucleotides -810 and -128 of the beta-globin locus, and the 3' breakpoint between the Ava II and Xmn I sites located downstream of the beta-globin gene. The father transmitted a codon 17 nonsense mutation, a beta-thalassemia variant common in Thailand, to the child.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Composition / physiology
  • Base Sequence
  • Child
  • Chromosome Deletion*
  • DNA / genetics
  • Female
  • Globins / genetics*
  • Humans
  • Molecular Sequence Data
  • Mutation
  • Nucleic Acid Hybridization
  • Restriction Mapping
  • Thailand
  • Thalassemia / genetics*

Substances

  • Globins
  • DNA