论文信息 - Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome) - 字舞流文

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

L. Wain | M. Tobin | I. Hall | A. Henry | S. Cook | J. Ware | M. Stowasser | R. Gordon | M. Glover | Shengxin Xu | R. Walsh | W. V. van’t Hoff | M. Wolley | K. O’Shaughnessy