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β-Thalassaemia Major in a Spanish Patient due to a Compound Heterozygosity for CD39 C→T/−28 A→C
oleh: Soledad Gamarra, Guillermo Garcia-Effron, Carmen Monteserin, Isabel Lopez-Villar, Florinda Gilsanz, Joaquín Martinez-Lopez
Format: | Article |
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Diterbitkan: | Wiley 2009-01-01 |
Deskripsi
A Spanish male patient with β-thalassaemia major was studied. Compound heterozygosity was found for one of the most common β-globin gene mutations in the Spanish population (codon 39 C→T) and for a mutation in the TATA box element of the β-globin gene promoter (−28 A→C mutation). To our knowledge this is the first report of a CD39 C→T and −28 A→C change association and the first report of the −28 A→C substitution in a Spanish patient.