A β-Thalassemia Mutation Found in Korea
- 1 January 1992
- journal article
- case report
- Published by Taylor & Francis in Hemoglobin
- Vol. 16 (4) , 313-320
- https://doi.org/10.3109/03630269208998875
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- A New β-Thalassemia Mutation (Initiation Codon ATG→GTG) Found in the Japanese PopulationHemoglobin, 1991
- Regulation of γ‐Globin Expression in Hereditary Persistence of Fetal HemoglobinAnnals of the New York Academy of Sciences, 1990
- An Initiation Codon Mutation as a Cause of a β-ThalassemiaHemoglobin, 1990
- β-Thalassehia RepositoryHemoglobin, 1989
- Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probesNature, 1986
- Comparison of initiation of protein synthesis in procaryotes, eucaryotes, and organelles.Microbiological Reviews, 1983
- Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene clusterNature, 1982
- Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin GenesHemoglobin, 1981
- DNA sequencing with chain-terminating inhibitorsProceedings of the National Academy of Sciences, 1977