Organization of α-globin genes in Hb Hasharon (α 47asp→his) carriers

B. Giglioni, P. Comi, R. Taramelli, S. Ottolenghi, M. A. Ciocca-Vasino, C. Anè, M. D. Cappellini, A. M. Gianni

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Abstract

Restriction enzymes analysis of the DNA from two unrelated Italian families with Hb Hasharon, a variant Hb (α 47asp→his) frequently occurring in the Polesine area in Italy, indicates that this variant is associated to an α globin gene deletion. The α(Hash) genotype most likely results from a mutation on an α thal 2 genotype.

Original languageEnglish
Pages (from-to)1145-1149
Number of pages5
JournalBlood
Volume56
Issue number6
Publication statusPublished - 1980

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ASJC Scopus subject areas

  • Hematology

Cite this

Giglioni, B., Comi, P., Taramelli, R., Ottolenghi, S., Ciocca-Vasino, M. A., Anè, C., Cappellini, M. D., & Gianni, A. M. (1980). Organization of α-globin genes in Hb Hasharon (α 47asp→his) carriers. Blood, 56(6), 1145-1149.