Unusual extramedullary relapses under imatinib mesylate treatment in chronic myeloid leukemia |
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Authors: | Beyazit Yavuz Aksu Salih Kekilli Murat Haznedaroglu Ibrahim C Kilickap Sadettin Goker Hakan |
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Affiliation: | LAIKON General Hospital, Center for Thalassemia, Unit of Prenatal Diagnosis, Athens, Greece. |
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Abstract: | There are at least four distinct African and one Asian chromosomal backgrounds (haplotypes) on which the sickle cell mutation has arisen. Additionally, previous data suggest that the beta(S)/Bantu haplotype is heterogeneous at the molecular level. Here, we report the presence of the (A)gamma -499 T-->A variation in sickle cell anemia chromosomes of Sicilian and North African origin bearing the beta(S)/Benin haplotype. Being absent from North American beta(S)/Benin chromosomes, which were studied previously, this variation is indicative for the molecular heterogeneity of the beta(S)/Benin haplotype. |
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Keywords: | sickle cell anemia βS/Benin haplotype γ‐globin genes DGGE |
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