Nucleic Acids Research, 1981, Vol. 9, No. 24 6813-6825
© 1981
MOLECULAR BIOLOGY |
Restriction mapping of a new deletion responsible for G
(
ß)° thalassaemia
MRC Molecular Haematology Unit, Nuffield Department of Clinical Medicine, John Radcliffe Hospital Oxford 0X3 9DU, UK
Received September 21, 1981.
DNA from individuals heterozygous for G
(
ß)° thalassaemia has been studied by restriction endonuclease analysis. The results reveal a new molecular defect associated with this condition. A total of three defects is now responsible for the one single phenotype, thereby emphasising the complex relationship between genotype and phenotype among the disorders of ß-like globin synthesis in man.
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