एपीए उद्धरण

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.

शिकागो स्टाइल उद्धरण

Glover, 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.

एमएलए उद्धरण

Glover, 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.