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Hb Belfast [beta15(A12)Trp-->Arg]: definition of the clinical and hematological phenotype
Renzo Galanello1, Lucia Perseu, Susanna Barella
1Dipartimento di Scienze Biomediche e Biotecnologie, Università degli Studi di Cagliari, Cagliari, Italia. renzo.galanello@mcweb.unica.it
Abstract:
We report the sixth occurrence of Hb Belfast [beta15(A12)Trp-->Arg], a mild, unstable beta chain variant, in a large family wherein nine subjects were affected. DNA analysis showed a TUG-->AGG mutation at codon 15 of the beta-globin gene, confirming a Trp-->Arg amino acid substitution. The oxygen affinity of the isolated variant was increased. The clinical phenotype is silent or very mild, the only clinical finding being an intermittent moderate jaundice.
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