Skip to Main Content

Paper Details

Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation.
Medicine (Baltimore)
4
2018
Atherosclerosis, FHS, KCNJ1, NCCT, NKCC2, ROMK, SLC12A1, SLC12A3, electrolyte abnormalities, exome, human, human sequences, hypertension, hypotension syndrome, hypotension syndromes, orthologs, participants, rare coding variants, rare variants, renal salt handling genes

Datasets

Release 1.2