Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome).
Clinical science (London, England : 1979) | 2014-05-01 | PMID 24266877
Glover Mark, Ware James S, Henry Amanda and 11 more
Genes: CUL3, KLHL3, WNK1, WNK4
