Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/82318
Title: Globin gene organisation and expression
Authors: Zhao, J.
Chui, D. H. K.
Felice, Alex
Keywords: Hemoglobin
Hemoglobinopathy
Sickle cell anemia
Molecular microbiology
Issue Date: 1987
Publisher: American Society of Hematology
Citation: Zhao, J., Chui, D. H. K., & Felice, A. (1987). Globin gene organisation and expression. Twenty-ninth Annual Meeting of the American Society of Hematology, Washington, DC. 82a.
Abstract: Re-arranqement of the α and ζ qlobin qenea are rather common in Black Americans. Two variants of the -3.7 Kb α qlobin qene deletion occur with a qene frequency of 0.18 while four variants of a ζ qlobin qene deletion occur in 3% of the population with or without α-thalassemia. Another type of ζ qene deletion occurs in the context of a (ζα) -thalassemia in which all α and ζ qlobin qenes are deleted. Further variability of ζ globin genes is due to dimorphism of the ζ 1 or ψζ, 1 genes.
URI: https://www.um.edu.mt/library/oar/handle/123456789/82318
Appears in Collections:Scholarly Works - FacM&SSur

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