Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/101634
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.
Editor: 
Rights: fechado
Identifier DOI: 10.1034/j.1600-0609.2002.02743.x
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0036757763&partnerID=40&md5=54aa4559eda365a7fafd9cf786d2bdc1
Date Issue: 2002
Appears in Collections:Unicamp - Artigos e Outros Documentos

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