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Hb Florida: A novel elongated C-terminal β-globin variant causing dominant β-thalassemia phenotype

✍ Scribed by B.I. Weinstein; B. Erramouspe; D.M. Albuquerque; D.M. Oliveira; E.M. Kimura; F.F. Costa; M.F. Sonati


Book ID
101437431
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
189 KB
Volume
81
Category
Article
ISSN
0361-8609

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A novel β-globin structural mutant, Hb B
✍ S. Murru; D. Poddie; G. V. Sciarratta; S. Agosti; M. Baffico; C. Melevendi; M. P 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 393 KB

This study describes a patient with a thalassemia intermedia-like phenotype in whom P-globin gene sequencing detected a novel abnormal hemoglobin (Hb) due to a T-C substitution at codon 114 of the P-globin gene arising as a de novo mutation. The abnormal variant was designated Hb Brescia after the p