Hemoglobin H disease resulting from the association of the - alpha(3.7) rightward deletion and the (alpha alpha)(MM) deletion in a Brazilian patient

dc.creatorWenning, MRSC
dc.creatorHarteveld, CL
dc.creatorGiordano, PC
dc.creatorKimura, EM
dc.creatorSaad, STO
dc.creatorCosta, FF
dc.creatorSonati, MF
dc.date2002
dc.dateSEP
dc.date2014-11-18T21:09:22Z
dc.date2015-11-26T17:54:22Z
dc.date2014-11-18T21:09:22Z
dc.date2015-11-26T17:54:22Z
dc.date.accessioned2018-03-29T00:38:00Z
dc.date.available2018-03-29T00:38:00Z
dc.identifierEuropean Journal Of Haematology. Blackwell Munksgaard, v. 69, n. 3, n. 179, n. 181, 2002.
dc.identifier0902-4441
dc.identifierWOS:000178849000008
dc.identifier10.1034/j.1600-0609.2002.02743.x
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/68240
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/68240
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/68240
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1290771
dc.descriptionA 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.
dc.description69
dc.description3
dc.description179
dc.description181
dc.languageen
dc.publisherBlackwell Munksgaard
dc.publisherCopenhagen
dc.publisherDinamarca
dc.relationEuropean Journal Of Haematology
dc.relationEur. J. Haematol.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjecthemoglobin H disease
dc.subjectalpha-thalassemia
dc.subjectalpha-globin genes
dc.subjectalpha-major regulatory element
dc.subjectSouth-American population
dc.subjectGlobin Gene
dc.subjectThalassemia
dc.subjectMutations
dc.subjectLocus
dc.titleHemoglobin H disease resulting from the association of the - alpha(3.7) rightward deletion and the (alpha alpha)(MM) deletion in a Brazilian patient
dc.typeArtículos de revistas


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