Two β-Thalassemia Mutations in Japan: Codon 121 (Gaa→Taa) and IVS-I-130 (G→C)

This publication has 14 references indexed in Scilit:

• Three β-Thalassemia Mutations in the Japanese: IVS-II-1 (G→A). IVS-II-848 (C→G), and Cooon 90 (GAG→TAG)
  Hemoglobin, 1992
• Molecular basis for dominantly inherited inclusion body beta-thalassemia.
  Proceedings of the National Academy of Sciences, 1990
• β-Thalassemia in Turkey
  Hemoglobin, 1990
• One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain [letter]
  Blood, 1989
• Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114
  Blood, 1988
• Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes
  Nature, 1986
• Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
  Nature, 1982
• Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin Genes
  Hemoglobin, 1981
• DNA sequencing with chain-terminating inhibitors
  Proceedings of the National Academy of Sciences, 1977
• Inclusion-Body β-Thalassemia Trait
  New England Journal of Medicine, 1974