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β‐Globin gene cluster haplotypes and α‐thalassemia in sickle cell disease patients from Trinidad
Authors:Altheia Jones‐Lecointe,Erskine Smith,Marc Romana,Marie‐Georges Gilbert,Waveney P. Charles,Christian Saint‐Martin,Lisiane Ké  clard
Abstract:
In this study, we have determined the frequency of βS haplotypes in 163 sickle cell disease patients from Trinidad. The α3.7 globin gene deletion status was also studied with an observed gene frequency of 0.17. Among the 283 βS chromosomes analyzed, the Benin haplotype was the most prevalent (61.8%) followed by Bantu (17.3%), Senegal (8.5%), Cameroon (3.5%), and Arab‐Indian (3.2%), while 5.7% of them were atypical. This βS haplotypes distribution differed from those previously described in other Caribbean islands (Jamaica, Guadeloupe, and Cuba), in agreement with the known involvement of the major colonial powers (Spain, France, and Great Britain) in the slave trade in Trinidad and documented an Indian origin of the βS gene. Am. J. Hum. Biol., 2008. © 2008 Wiley‐Liss, Inc.
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