導出完成 — 

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

10.1042/CS20130326

Saved in:
書目詳細資料
Main Authors: 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.
其他作者: DUKE-NUS MEDICAL SCHOOL
格式: Article
出版: 2019
主題:
在線閱讀:http://scholarbank.nus.edu.sg/handle/10635/150853
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!
機構: National University of Singapore