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Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.
Akinbami, Anthony O; Campbell, Andrew D; Han, Zeqiu J; Luo, Hong-Yuan; Chui, David H K; Steinberg, Martin H.
Afiliação
  • Akinbami AO; a Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA.
  • Campbell AD; b Department of Pediatrics , University of Michigan , Ann Arbor , Michigan , USA.
  • Han ZJ; c Quest Diagnostics Nichols Institute , Chantilly , Virginia , USA.
  • Luo HY; a Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA.
  • Chui DH; a Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA.
  • Steinberg MH; a Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA.
Hemoglobin ; 40(1): 64-5, 2016.
Article em En | MEDLINE | ID: mdl-26372199
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Traço Falciforme / Hemoglobina Fetal / Hemoglobina Falciforme / Mutação Puntual / Gama-Globinas / Doença da Hemoglobina SC Limite: Adult / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Traço Falciforme / Hemoglobina Fetal / Hemoglobina Falciforme / Mutação Puntual / Gama-Globinas / Doença da Hemoglobina SC Limite: Adult / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article