Artículos de revistas
Hemoglobin H Disease Resulting From The Association Of The - Alpha 3.7 Rightward Deletion And The (alpha Alpha)mm Deletion In A Brazilian Patient.
Registro en:
European Journal Of Haematology. v. 69, n. 3, p. 179-81, 2002-Sep.
0902-4441
12406012
Autor
Wenning, M R S C
Harteveld, C L
Giordano, P C
Kimura, E M
Saad, S T O
Costa, F F
Sonati, M F
Institución
Resumen
A patient with Hb H disease resulting from the association of the - alpha 3.7 rightward deletion with the rare (alpha alpha)MM deletion, which removes the entire alpha-major regulatory element (MRE), is reported. This is the first description of an alpha-thalassemic mutation resulting from deletion of the locus-controlling sequences in the South-American population. 69 179-81