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Whole-exome sequencing identified mutational profile of a case with T-cell chronic lymphocytic leukemia.
Nozaki, Kenji; Yokota, Takafumi; Itotagawa, Eri; Tsutsumi, Kazuhito; Kusakabe, Shinsuke; Morikawa, Yoichiro; Fujita, Jiro; Fukushima, Kentaro; Maeda, Tetsuo; Shibayama, Hirohiko; Hosen, Naoki; Kumanogo, Atsushi; Kanakura, Yuzuru.
Afiliação
  • Nozaki K; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Yokota T; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Itotagawa E; Department of Respiratory Medicine and Clinical Immunology Graduate School of Medicine Osaka University Suita Japan.
  • Tsutsumi K; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Kusakabe S; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Morikawa Y; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Fujita J; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Fukushima K; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Maeda T; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Shibayama H; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Hosen N; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
  • Kumanogo A; Department of Respiratory Medicine and Clinical Immunology Graduate School of Medicine Osaka University Suita Japan.
  • Kanakura Y; Department of Hematology and Oncology Osaka University Graduate School of Medicine Suita Japan.
Clin Case Rep ; 8(11): 2251-2254, 2020 Nov.
Article em En | MEDLINE | ID: mdl-33235770
We believe that our report and further case reports on T-cell chronic lymphocytic leukemia with genetic profile will contribute to the molecular classification of this rare but distinct disease.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article