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

Ihsan TuranLeman Damla KotanMehmet TastanFatih GurbuzAli Kemal TopalogluBilgin Yuksel

Published in: Clinical endocrinology (2018)

Molecular genetic investigations can help confidently diagnose these conditions and clarify the pathogenicity of aldosterone defects. This study may expand the clinical and genetic correlations of defects in aldosterone synthesis or resistance.

Keyphrases

genome wide
angiotensin ii
copy number
single molecule
dna methylation
gene expression
escherichia coli
biofilm formation
case control
candida albicans