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A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency.
Firtina, Sinem; Cipe, Funda; Ng, Yuk Yin; Kiykim, Ayca; Ng, Ozden Hatirnaz; Sudutan, Tugce; Aydogmus, Cigdem; Baris, Safa; Ozturk, Gulyuz; Aydiner, Elif; Ozen, Ahmet; Sayitoglu, Muge.
Afiliación
  • Firtina S; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
  • Cipe F; Department of Molecular Biology and Genetics, Istinye University, Istanbul, Turkey.
  • Ng YY; Department of Pediatric Allergy and Infection, Istanbul Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
  • Kiykim A; Department of Genetics and Bioengineering, Istanbul Bilgi University, Istanbul, Turkey.
  • Ng OH; Department of Pediatric Allergy and Infection, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.
  • Sudutan T; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
  • Aydogmus C; Department of Medical Biology, Acibadem Mehmet Ali Aydinlar University Medical Faculty Istanbul, Istanbul, Turkey.
  • Baris S; Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
  • Ozturk G; Department of Pediatric Allergy and Infection, Istanbul Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey.
  • Aydiner E; Department of Pediatric Allergy and Immunology, Marmara University, Istanbul, Turkey.
  • Ozen A; Pediatric Bone Marrow Transplantation Unit, Acibadem Atakent Hospital, Istanbul, Turkey.
  • Sayitoglu M; Department of Pediatric Allergy and Immunology, Marmara University, Istanbul, Turkey.
J Clin Immunol ; 39(2): 144-147, 2019 02.
Article en En | MEDLINE | ID: mdl-30903456
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunodeficiencia Combinada Grave / Factores de Transcripción Forkhead Tipo de estudio: Prognostic_studies Límite: Female / Humans / Infant / Male País/Región como asunto: Asia Idioma: En Revista: J Clin Immunol Año: 2019 Tipo del documento: Article País de afiliación: Turquía
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inmunodeficiencia Combinada Grave / Factores de Transcripción Forkhead Tipo de estudio: Prognostic_studies Límite: Female / Humans / Infant / Male País/Región como asunto: Asia Idioma: En Revista: J Clin Immunol Año: 2019 Tipo del documento: Article País de afiliación: Turquía