A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.

MLA

Feriotto, Giordana, et al. “A Novel Frameshift Mutation (+A) at Codon 18 of the Beta-Globin Gene Associated with High Persistence of Fetal Hemoglobin Phenotype and Deltabeta-Thalassemia.” Acta Haematologica, vol. 119, no. 1, 2008, pp. 28–37. EBSCOhost, https://doi.org/10.1159/000114204.

APA

Feriotto, G., Salvatori, F., Finotti, A., Breveglieri, G., Venturi, M., Zuccato, C., Bianchi, N., Borgatti, M., Lampronti, I., Mancini, I., Massei, F., Favre, C., & Gambari, R. (2008). A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia. Acta Haematologica, 119(1), 28–37. https://doi.org/10.1159/000114204

Chicago

Feriotto, Giordana, Francesca Salvatori, Alessia Finotti, Giulia Breveglieri, Marina Venturi, Cristina Zuccato, Nicoletta Bianchi, et al. 2008. “A Novel Frameshift Mutation (+A) at Codon 18 of the Beta-Globin Gene Associated with High Persistence of Fetal Hemoglobin Phenotype and Deltabeta-Thalassemia.” Acta Haematologica 119 (1): 28–37. doi:10.1159/000114204.