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Novel mechanism of hereditary pyropoikilocytosis phenotype due to co-inheritance of ß globin and α spectrin mutations.
Kim, Soo Jin; Song, Jihyun; Reading, N Scott; Lautersztain, Julio; Kutlar, Abdullah; Agarwal, Archana M; Coetzer, Theresa L; Prchal, Josef T.
Afiliação
  • Kim SJ; Hematology, University of Utah & Huntsman Cancer Center, Salt Lake City, Utah.
  • Song J; Hematology, University of Utah & Huntsman Cancer Center, Salt Lake City, Utah.
  • Reading NS; Department of Pathology, ARUP Laboratories, Salt Lake City, Utah.
  • Lautersztain J; Florida Cancer Specialists and Research Institute, Tampa, Florida.
  • Kutlar A; Medical College of Georgia, Augusta, Georgia.
  • Agarwal AM; Department of Pathology, ARUP Laboratories, Salt Lake City, Utah.
  • Coetzer TL; Department of Molecular Medicine and Haematology, School of Pathology, University of the Witwatersrand, Johannesburg, South Africa.
  • Prchal JT; Hematology, University of Utah & Huntsman Cancer Center, Salt Lake City, Utah.
Am J Hematol ; 96(5): E150-E154, 2021 05 01.
Article em En | MEDLINE | ID: mdl-33556202
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mutação da Fase de Leitura / Espectrina / Mutação Puntual / Eliptocitose Hereditária / Globinas beta Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mutação da Fase de Leitura / Espectrina / Mutação Puntual / Eliptocitose Hereditária / Globinas beta Idioma: En Ano de publicação: 2021 Tipo de documento: Article