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, vol.88, pp.799-805, 2018 (SCI-Expanded, Scopus) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 88
  • Publication Date: 2018
  • Doi Number: 10.1111/cen.13603
  • Journal Name: Clinical endocrinology
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.799-805
  • Keywords: CYP11B2, ENaC, hypoaldosteronism, isolated hypoaldosteronism, novel mutations, NR3C2, pseudohypoaldosteronism, HUMAN MINERALOCORTICOID RECEPTOR, PSEUDOHYPOALDOSTERONISM TYPE-1, MISSENSE MUTATION, IDENTIFICATION, VARIANTS, CLONING, INFANT, SCNN1A, FAMILY
  • Çukurova University Affiliated: Yes