beta-thalassemia intermedia in a Brazilian patient with - 101(C > T) and codon 39 (C > T) mutations

CONTEXT: We verified molecular alterations in a 72-year-old Brazilian male patient with a clinical course of homozygous beta-thalassemia intermedia, who had undergone splenectomy and was surviving without regular blood transfusions. The blood cell count revealed microcytic and hypochromic anemia (he...

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Hlavní autoři:	Sylvia Morais de Sousa, Letícia Khater, Luís Antônio Peroni, Karine Miranda, Marcelo Jun Murai, Dulcinéia Martins Albuquerque, Paulo Arruda, Sara Terezinha Ollala Saad, Fernando Ferreira Costa
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Associação Paulista de Medicina
Edice:	São Paulo Medical Journal
Témata:	Beta thalassemia Mutations Beta globin
On-line přístup:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802003000100007&lng=en&tlng=en
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