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

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Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)..pdf (902.16 KB)

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Author(s)

Glover, M

Ware, JS

Henry, A

Wolley, M

Walsh, R

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Type

Journal Article

Date Issued

2014-05-01

URI

http://hdl.handle.net/10044/1/25549

DOI

http://dx.doi.org/10.1042/CS20130326

ISSN

0143-5221

Publisher

PORTLAND PRESS LTD

Start Page

721

End Page

726

Journal / Book Title

CLINICAL SCIENCE

Volume

126

Issue

9-10

Copyright Statement

© 2014 The author(s). This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited.

License URL

https://creativecommons.org/licenses/by/4.0/

Identifier

http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000335284000012&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202

Publication Status

Published