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Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2
Turan, Hande; Dagdeviren Çakir, Aydilek; Özer, Yavuz; Tarçin, Gürkan; Özcabi, Bahar; Ceylaner, Serdar; Ercan, Oya; Evliyaoglu, Saadet Olcay.
Afiliação
  • Turan H; Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Department of Pediatric Endocrinology, Istanbul, Turkey
  • Dagdeviren Çakir A; Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Department of Pediatric Endocrinology, Istanbul, Turkey
  • Özer Y; Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Department of Pediatric Endocrinology, Istanbul, Turkey
  • Tarçin G; Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Department of Pediatric Endocrinology, Istanbul, Turkey
  • Özcabi B; Zeynep Kamil Training and Research Hospital, Clinic of Pediatric Endocrinology, Istanbul, Turkey
  • Ceylaner S; Intergen Genetic Diagnosis Center, Medical Genetics, Ankara, Turkey
  • Ercan O; Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Department of Pediatric Endocrinology, Istanbul, Turkey
  • Evliyaoglu SO; Istanbul University-Cerrahpasa, Cerrahpasa Faculty of Medicine, Department of Pediatric Endocrinology, Istanbul, Turkey
J Clin Res Pediatr Endocrinol ; 13(2): 232-238, 2021 06 02.
Article em En | MEDLINE | ID: mdl-32539318

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipoaldosteronismo / Citocromo P-450 CYP11B2 Tipo de estudo: Prognostic_studies / Screening_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipoaldosteronismo / Citocromo P-450 CYP11B2 Tipo de estudo: Prognostic_studies / Screening_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article