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Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor ß1 and biotinidase deficiencies.
Dogruel, Dilek; Bulut, Fatma Derya; Yilmaz, Mustafa; Önenli-Mungan, Neslihan; Altintas, Derya Ufuk.
Affiliation
  • Dogruel D; Division of Allergy and Immunology, Çukurova University Faculty of Medicine, Adana, Turkey.
  • Bulut FD; Metabolism and Nutrition, Department of Pediatrics, Çukurova University Faculty of Medicine, Adana, Turkey.
  • Yilmaz M; Division of Allergy and Immunology, Çukurova University Faculty of Medicine, Adana, Turkey.
  • Önenli-Mungan N; Metabolism and Nutrition, Department of Pediatrics, Çukurova University Faculty of Medicine, Adana, Turkey.
  • Altintas DU; Division of Allergy and Immunology, Çukurova University Faculty of Medicine, Adana, Turkey.
Turk J Pediatr ; 60(5): 584-587, 2018.
Article in En | MEDLINE | ID: mdl-30968642
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biotinidase Deficiency / Receptors, Interleukin-12 / Immunologic Deficiency Syndromes Limits: Female / Humans / Infant / Newborn Language: En Journal: Turk J Pediatr Year: 2018 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biotinidase Deficiency / Receptors, Interleukin-12 / Immunologic Deficiency Syndromes Limits: Female / Humans / Infant / Newborn Language: En Journal: Turk J Pediatr Year: 2018 Document type: Article Affiliation country: Country of publication: