Your browser doesn't support javascript.
loading
Inherited transmission of the CSF3R T618I mutational hotspot in familial chronic neutrophilic leukemia.
Duployez, Nicolas; Willekens, Christophe; Plo, Isabelle; Marceau-Renaut, Alice; de Botton, Stéphane; Fenwarth, Laurène; Boyer, Thomas; Huet, Guillemette; Nibourel, Olivier; Rose, Christian; Nelken, Brigitte; Quesnel, Bruno; Preudhomme, Claude.
Afiliação
  • Duployez N; Laboratory of Hematology, Biology and Pathology Center, CHU Lille, Lille, France.
  • Willekens C; University of Lille, INSERM UMR-S 1172, Lille, France.
  • Plo I; Department of Hematology, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
  • Marceau-Renaut A; Université Paris-Sud 11, INSERM U1170, Villejuif, France.
  • de Botton S; Université Paris-Sud 11, INSERM U1170, Villejuif, France.
  • Fenwarth L; Laboratory of Hematology, Biology and Pathology Center, CHU Lille, Lille, France.
  • Boyer T; University of Lille, INSERM UMR-S 1172, Lille, France.
  • Huet G; Department of Hematology, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
  • Nibourel O; Université Paris-Sud 11, INSERM U1170, Villejuif, France.
  • Rose C; Laboratory of Hematology, Biology and Pathology Center, CHU Lille, Lille, France.
  • Nelken B; University of Lille, INSERM UMR-S 1172, Lille, France.
  • Quesnel B; Laboratory of Hematology, Biology and Pathology Center, CHU Lille, Lille, France.
  • Preudhomme C; University of Lille, INSERM UMR-S 1172, Lille, France.
Blood ; 134(26): 2414-2416, 2019 12 26.
Article em En | MEDLINE | ID: mdl-31697825

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Neutrofílica Crônica / Receptores de Fator Estimulador de Colônias / Predisposição Genética para Doença / Mutação Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Neutrofílica Crônica / Receptores de Fator Estimulador de Colônias / Predisposição Genética para Doença / Mutação Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article