Συγγραφείς:
Traeger-Synodinos, J.
Bosch, C.A.J.
Vrettou, C.
Maragoudaki, L.
Apostolidis, J.
Kanavakis, E.
Kattamis, C.
Arkesteijn, S.G.J.
Hoffer, M.J.V.
Ruivenkamp, C.A.L.
Harteveld, C.L.
Λέξεις-κλειδιά:
adult; adult disease; beta thalassemia; beta thalassemia intermedia; case report; clinical article; clonal variation; female; gene; gene deletion; HBB gene; hematopoietic stem cell; homozygosity; human; human cell; Letter; middle aged; onset age; priority journal; Sanger sequencing; segmental duplication; somatic mutation; beta thalassemia; blood; gene deletion; gene locus; genetics; multigene family; nucleotide sequence, hemoglobin beta chain, Adult; Age of Onset; Base Sequence; beta-Globins; beta-Thalassemia; Female; Genetic Loci; Humans; Multigene Family; Sequence Deletion
