Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance.


TURAN İ., Kotan L. D., TASTAN M., GURBUZ F., TOPALOĞLU A. K., YÜKSEL B.

Clinical endocrinology, cilt.88, ss.799-805, 2018 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 88
  • Basım Tarihi: 2018
  • Doi Numarası: 10.1111/cen.13603
  • Dergi Adı: Clinical endocrinology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.799-805
  • Anahtar Kelimeler: CYP11B2, ENaC, hypoaldosteronism, isolated hypoaldosteronism, novel mutations, NR3C2, pseudohypoaldosteronism, HUMAN MINERALOCORTICOID RECEPTOR, PSEUDOHYPOALDOSTERONISM TYPE-1, MISSENSE MUTATION, IDENTIFICATION, VARIANTS, CLONING, INFANT, SCNN1A, FAMILY
  • Çukurova Üniversitesi Adresli: Evet