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Hemoglobin
international journal for hemoglobin research
Volume 44, 2020 - Issue 4
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Short Communications

Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes

Salvador Payán-Perníaa Hematology Department, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain;b National Reference Center (CSUR) for Hereditary Red Blood Cell Disorders, Hospital Sant Joan de Déu-Hospital de la Santa Creu i Sant Pau, Barcelona, SpainCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0002-4288-7362
ORCID Icon,
Sara Bernal Noguerab National Reference Center (CSUR) for Hereditary Red Blood Cell Disorders, Hospital Sant Joan de Déu-Hospital de la Santa Creu i Sant Pau, Barcelona, Spain;c Genetics Department, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain;d U705 for Biomedical Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain
,
Esther Rojas Rodríguezb National Reference Center (CSUR) for Hereditary Red Blood Cell Disorders, Hospital Sant Joan de Déu-Hospital de la Santa Creu i Sant Pau, Barcelona, Spain;c Genetics Department, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain
,
Marta Serra Ferrera Hematology Department, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain;b National Reference Center (CSUR) for Hereditary Red Blood Cell Disorders, Hospital Sant Joan de Déu-Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
&
Ángel F. Remacha Sevillaa Hematology Department, Hospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain;b National Reference Center (CSUR) for Hereditary Red Blood Cell Disorders, Hospital Sant Joan de Déu-Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
Pages 294-296 | Received 14 Jan 2020, Accepted 08 Jun 2020, Published online: 21 Jul 2020

References

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  • Altay C, Oner C, Oner R, et al. Effect of α-gene numbers on the expression of β-thalassemia intermedia, β-thalassemia and (δβ)0-thalassemia traits. Hum Hered. 1998;48(3):121–125.

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