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Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins.
Alrumayyan, Nora; Slauenwhite, Drew; McAlpine, Sarah M; Roberts, Sarah; Issekutz, Thomas B; Huber, Adam M; Liu, Zaiping; Derfalvi, Beata.
Afiliación
  • Alrumayyan N; Division of Immunology, Department of Paediatrics, Dalhousie University, IWK Health Centre, Halifax, Canada.
  • Slauenwhite D; Division of Immunology, Department of Paediatrics, Dalhousie University, IWK Health Centre, Halifax, Canada.
  • McAlpine SM; Division of Immunology, Department of Paediatrics, Dalhousie University, IWK Health Centre, Halifax, Canada.
  • Roberts S; Division of Immunology, Department of Paediatrics, Dalhousie University, IWK Health Centre, Halifax, Canada.
  • Issekutz TB; Division of Immunology, Department of Paediatrics, Dalhousie University, IWK Health Centre, Halifax, Canada.
  • Huber AM; Division of Rheumatology, Department of Paediatrics, Dalhousie University, IWK Health Centre, Halifax, Canada.
  • Liu Z; Division of Clinical Biochemistry & Maritime Newborn Screening, Department of Pathology and Laboratory Medicine, Dalhousie University, IWK Health Centre, Halifax, Canada.
  • Derfalvi B; Division of Immunology, Department of Paediatrics, Dalhousie University, IWK Health Centre, Halifax, Canada. beata.derfalvi@iwk.nshealth.ca.
Allergy Asthma Clin Immunol ; 18(1): 17, 2022 Feb 23.
Article en En | MEDLINE | ID: mdl-35197125
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Allergy Asthma Clin Immunol Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Allergy Asthma Clin Immunol Año: 2022 Tipo del documento: Article