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Phenotypic evaluations of HBB:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin gene

Authors

  • Margherita Vinciguerra Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Filippo Cassarà Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Monica Cannata Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Disma Renda Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Giuseppina Calvaruso Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Filippo Leto Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Cristina Passarello Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Aurelio Maggio Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  • Antonino Giambona Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Antonino Giambona, Department of Hematology for Rare Diseases of Blood and Blood-forming Organs, Laboratory for Molecular Diagnosis of Rare Diseases, Villa Sofia-Cervello Hospital, Palermo, Italy; a.giambona{at}villasofia.it
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Citation

Vinciguerra M, Cassarà F, Cannata M, et al
Phenotypic evaluations of HBB:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin gene

Publication history

  • Received June 30, 2017
  • Revised July 14, 2017
  • Accepted July 19, 2017
  • First published August 9, 2017.
Online issue publication 
March 20, 2018

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