Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/82525
Title: Quantification of in-vivo : expression of the β-IVS-I-NT#6 thalassaemia mutation
Authors: Felice, Alex
Abela, W.
Bartolo, C.
Borg, I.
Camilleri, R.
Grech, J. L.
Pizzuto, M.
Scerri, Christian A.
Keywords: Hemoglobin
Hemoglobinopathy
Thalassemia
Molecular microbiology
Issue Date: 1991
Citation: Felice, A., Abela, W., Bartolo, C., Borg, I., Camilleri, R., Grech, J. L., Pizzuto, M., & Scerri, C. (1991). Quantification of in-vivo : expression of the β-IVS-I-NT#6 thalassaemia mutation. 4th International Conference on Thalassaemia and the Haemoglobinopathies, Nice. 101.
Abstract: A recently described β chain variant, Hb Valletta (or α2β287PRO; Felice .at aJ., BLOOD, 74, 7, suppl. 1, 141a, 1989) has been observed among 1.8% of the Maltese population among whom β+ & βo thal occur with a combined heterozygous incidence of 2.4 %. This provides an opportunity to quantify objectively, through the proportion of Hb A or of β(A) chains in double heterozygotes, the degree of functional deficit due to the β+ thal mutations which prevail in this area.
URI: https://www.um.edu.mt/library/oar/handle/123456789/82525
Appears in Collections:Scholarly Works - FacM&SSur

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