β-Thalassemia in four Mediterranean Countries; an Editorial Commentary
1990; Taylor & Francis; Volume: 14; Issue: 1 Linguagem: Inglês
10.3109/03630269009002253
ISSN1532-432X
Autores Tópico(s)Blood groups and transfusion
ResumoPreceding papers provide detailed data about the occurrence of various β-thalassemia (thal) alleles in the populations of Turkey, Bulgaria, and Yugoslavia. A review of these results together with similar data for a large group of Greek children with β-thalassemia major allows a comparison of the frequencies of some of the more important mutations and frameshifts, as well as an evaluation of some of the clinical effects of (combinations of) different mutations
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