A Novel 13 BP Deletion in the 3′UTR of the β-Globin Gene Causes β-Thalassemia in a Turkish Patient

This publication has 14 references indexed in Scilit:

• The molecular basis of β-thalassemia in Turkey
  Human Genetics, 1992
• The β- and δ-Thalassemia Repository
  Hemoglobin, 1992
• The G→A Mutation at Position +22 3¹to the Cap Site of the β-Globin Gene as a Possible Cause for a β-Thalassemia
  Hemoglobin, 1991
• A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with “silent” beta-thalassemia
  Blood, 1989
• The poly(A)-poly(A)-binding protein complex is a major determinant of mRNA stability in vitro.
  Molecular and Cellular Biology, 1989
• Severe Hb S‐β°‐thalassaemia with a T → C substitution in the donor splice site of the first intron of the β‐globin gene
  British Journal of Haematology, 1989
• HB Monroe or α₂β₂30(B12)ARG→THR, a Variant Associated with β-Thalassemia due to a G→C Substitution Adjacent to the Donor Splice Site of the First Intron
  Hemoglobin, 1989
• Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus.
  Proceedings of the National Academy of Sciences, 1988
• Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States
  Blood, 1988
• The 3′ noncoding region of β-globin mRNA is not essential for in vitro translation
  Nucleic Acids Research, 1979