Glover, M., Ware, J., Henry, A., Wolley, M., Walsh, R., Wain, L., . . . O’Shaughnessy, K. (2014). Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). Portland Press Ltd.
Chicago Style CitationGlover, Mark, et al. Detection of Mutations in KLHL3 and CUL3 In families With FHHt (familial Hyperkalaemic Hypertension or Gordon's Syndrome). Portland Press Ltd, 2014.
MLA CitationGlover, Mark, et al. Detection of Mutations in KLHL3 and CUL3 In families With FHHt (familial Hyperkalaemic Hypertension or Gordon's Syndrome). Portland Press Ltd, 2014.
Warning: These citations may not always be 100% accurate.