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Detection of mutations inKLHL3andCUL3in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)
Detection of mutations inKLHL3andCUL3in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)
2014
Mark Glover
James S. Ware
Amanda P. Henry
Martin Wolley
Roddy Walsh
Louise V. Wain
Shengxin Xu
William van’t Hoff
Martin D. Tobin
Ian P. Hall
Stuart A. Cook
Richard D. Gordon
Michael Stowasser
Kevin M. OShaughnessy
Keywords:
Pediatrics
Internal medicine
Endocrinology
Diabetes mellitus
Medicine
Correction
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