Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/68240
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, MRSC
Harteveld, CL
Giordano, PC
Kimura, EM
Saad, STO
Costa, FF
Sonati, MF
Abstract: A patient with Hb H disease resulting from the association of the -alpha(3.7) rightward deletion with the rare (alphaalpha)(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: hemoglobin H disease
alpha-thalassemia
alpha-globin genes
alpha-major regulatory element
South-American population
Country: Dinamarca
Editor: Blackwell Munksgaard
Rights: fechado
Identifier DOI: 10.1034/j.1600-0609.2002.02743.x
Date Issue: 2002
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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