Detection of mutations in KLHL3 and CUL3 in families with Familial Hyperkalaemic Hypertension (FHH or Gordon syndrome)

Glover, M., Ware, J., Henry, A., Wolley, M., Xu, S., Cook, S., Hall, I, van't Hoff, W., Gordon, R., Stowasser, M. and O'Shaughnessy, K. (2013). Detection of mutations in KLHL3 and CUL3 in families with Familial Hyperkalaemic Hypertension (FHH or Gordon syndrome). In: 2013 Annual Scientific Meeting of the BHS, London United Kingdom, (638-638). 9th – 10th September 2013. doi:10.1038/jhh.2013.72


Author Glover, M.
Ware, J.
Henry, A.
Wolley, M.
Xu, S.
Cook, S.
Hall, I
van't Hoff, W.
Gordon, R.
Stowasser, M.
O'Shaughnessy, K.
Title of paper Detection of mutations in KLHL3 and CUL3 in families with Familial Hyperkalaemic Hypertension (FHH or Gordon syndrome)
Conference name 2013 Annual Scientific Meeting of the BHS
Conference location London United Kingdom
Conference dates 9th – 10th September 2013
Journal name Journal of Human Hypertension   Check publisher's open access policy
Place of Publication London United Kingdom
Publisher Nature Publishing Group
Publication Year 2013
Sub-type Published abstract
DOI 10.1038/jhh.2013.72
Open Access Status
ISSN 0950-9240
1476-5527
Volume 27
Issue 10
Start page 638
End page 638
Total pages 1
Language eng
Q-Index Code EX
Q-Index Status Provisional Code
Institutional Status UQ

Document type: Conference Paper
Collection: School of Medicine Publications
 
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Created: Sun, 13 Oct 2013, 00:03:37 EST by System User on behalf of School of Medicine