Common alpha globin genes (HBA1 and HBA2) mutations in Filipino patients with alpha thalassemia

Common alpha globin genes (HBA1 and HBA2) mutations in Filipino patients with alpha thalassemia

"Alpha (a) thalassemia results from the absence/reduced synthesis of the a-globin subunit of hemoglobin (Hb). Mutational variants in the HBA1 and HBA2, which code for a-globin, have been reported to cause varying degrees of disease severity. These variants are unique for every population. Howev...

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Detalles Bibliográficos
Publicado en:Vol. 150, No.2 (April 2021), pages 483-487.
Main Authors: Silao, Catherine Lynn T. (Author), Fabella, Terence Diane F. (Author), Naranjo, Maria Liza T. (Author), Barnuevo, Mayceemae M. (Author), Padilla, Carmencita D. (Author), Yuson, Ernesto dJ (Author)
Formato: Libro
Idioma:English
Subjects:
Blood > Analysis.
Gene expression.
Filipinos.
Hemoglobinopathy.