Detection of mutations in KLHL3 and CUL3 in families with fhht (familial hyperkalaemic hypertension or gordon's syndrome)

by Glover M., Ware J.S., Henry A., Wolley M., Walsh R., Wain L.V., Xu S., Hoff W.G.V., Tobin M.D., Hall I.P., Cook S., Gordon R.D., Stowasser M., O'shaughnessy K.M.
Published 2019

Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia

by Ware J.S., Wain L.V., Channavajjhala S.K., Jackson V.E., Edwards E., Lu R., Siew K., Jia W., Shrine N., Kinnear S., Jalland M., Henry A.P., Clayton J., O'Shaughnessy K.M., Tobin M.D., Schuster V.L., Cook S., Hall I.P., Glover M.
Published 2019