Your browser doesn't support javascript.
loading
Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome.
Aryan, Zahra; Nabavi, Mohammad; Shabani, Mahsima; Keles, Sevgi; Zoghi, Samaneh; Chatila, Talal; Rezaei, Nima.
Afiliación
  • Aryan Z; Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Nabavi M; Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran.
  • Shabani M; Primary Immunodeficiency Diseases Network (PIDNet), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
  • Keles S; Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
  • Zoghi S; Department of Allergy and Immunology, Rasool-e-Akram Hospital, Iran University of Medical Sciences, Tehran, Iran.
  • Chatila T; Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran.
  • Rezaei N; Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
Pediatr Blood Cancer ; 67(2): e28084, 2020 02.
Article en En | MEDLINE | ID: mdl-31749288
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Eliminación de Secuencia / Síndrome Hipereosinofílico / Factores de Intercambio de Guanina Nucleótido Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Child / Female / Humans Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2020 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Eliminación de Secuencia / Síndrome Hipereosinofílico / Factores de Intercambio de Guanina Nucleótido Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Child / Female / Humans Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2020 Tipo del documento: Article