Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Hemoglobin H Disease Resulting From The Association Of The - Alpha 3.7 Rightward Deletion And The (alpha Alpha)mm Deletion In A Brazilian Patient.
Author: Wenning, M R S C
Harteveld, C L
Giordano, P C
Kimura, E M
Saad, S T O
Costa, F F
Sonati, M F
Abstract: 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.
Subject: Adult
Gene Deletion
Citation: European Journal Of Haematology. v. 69, n. 3, p. 179-81, 2002-Sep.
Rights: fechado
Date Issue: 2002
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File SizeFormat 
pmed_12406012.pdf147.93 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.