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Unusual Prominent Pulmonary Involvement in a Homozygous PRF1 Gene Variant in a Female Patient.
Alsohime, Fahad; Almaghamsi, Talal; Basha, Talal A; Alardati, Hosam; Alghamdi, Malak; Hawsawi, Yousef Mohammed.
Afiliación
  • Alsohime F; Pediatric Intensive Care Unit, Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, PO Box: 7805, Pediatric number 39, Riyadh, 11472, Saudi Arabia. falsohime@ksu.edu.sa.
  • Almaghamsi T; Department of Pediatrics, King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia.
  • Basha TA; Pediatric Allergy-Immunology, Pediatric Department, Faculty of Medicine, University of Jeddah, Jeddah, Kingdom of Saudi Arabia.
  • Alardati H; Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia.
  • Alghamdi M; Pediatric Genetics and Metabolic Division, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
  • Hawsawi YM; Research Center, King Faisal Specialist Hospital and Research Center, P.O. Box 40047, Jeddah, 21499, Kingdom of Saudi Arabia.
J Clin Immunol ; 41(1): 217-220, 2021 01.
Article en En | MEDLINE | ID: mdl-32986178

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fenotipo / Predisposición Genética a la Enfermedad / Perforina / Homocigoto / Enfermedades Pulmonares / Mutación Tipo de estudio: Prognostic_studies Idioma: En Revista: J Clin Immunol Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fenotipo / Predisposición Genética a la Enfermedad / Perforina / Homocigoto / Enfermedades Pulmonares / Mutación Tipo de estudio: Prognostic_studies Idioma: En Revista: J Clin Immunol Año: 2021 Tipo del documento: Article