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 - α3.7 Rightward Deletion And The (αα)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 - α3.7 rightward deletion with the rare (αα)MM deletion, which removes the entire α-major regulatory element (MRE), is reported. This is the first description of an α-thalassemic mutation resulting from deletion of the locus-controlling sequences in the South-American population.
Rights: fechado
Identifier DOI: 10.1034/j.1600-0609.2002.02743.x
Date Issue: 2002
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
2-s2.0-0036757763.pdf147.93 kBAdobe PDFView/Open

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