Analysis of the A(TA)(n)TAA configuration in the promoter region of the UGT1 A1 gene in Greek patients with thalassemia intermedia and sickle cell disease

Gilbert's syndrome is characterized by mild unconjugated hyperbilirubinemia. The molecular basis of this syndrome usually concerns an additional dinucleotide insertion (TA) in the A(TA)(n)TAA configuration residing in the promoter region of the UGT1 A1 gene. This configuration may vary in lengt...

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Veröffentlicht in:	Blood cells, molecules, & diseases molecules, & diseases, 2003-07, Vol.31 (1), p.38-42
Hauptverfasser:	Kalotychou, Vassiliki, Antonatou, Katerina, Tzanetea, Revekka, Terpos, Evaggelos, Loukopoulos, Dimitris, Rombos, Yannis
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Sequence Anemia, Sickle Cell - blood Anemia, Sickle Cell - complications Anemia, Sickle Cell - genetics Bilirubin - blood Genotype Gilbert Disease - complications Gilbert Disease - genetics Glucuronosyltransferase - genetics Greece Humans Hyperbilirubinemia - etiology Hyperbilirubinemia - genetics Poly dA-dT - genetics Promoter Regions, Genetic Thalassemia - blood Thalassemia - complications Thalassemia - genetics
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