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, Scopus)

• 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