A New Kindred With Pseudohypoaldosteronism Type II and a Novel Mutation (564D>H) in the Acidic Motif of the WNK4 Gene-Reference-Cited by-同舟云学术

A New Kindred With Pseudohypoaldosteronism Type II and a Novel Mutation (564D>H) in the Acidic Motif of the WNK4 Gene

Published:2005-08 Issue:2 Volume:46 Page:295-300
ISSN:0194-911X
Container-title:Hypertension
language:en
Short-container-title:Hypertension

Author:

Golbang Amir P.¹,Murthy Meena¹,Hamad Abbas¹,Liu Che-Hsiung¹,Cope Georgina¹,Van’t Hoff William¹,Cuthbert Alan¹,O’Shaughnessy Kevin M.¹

Affiliation:

1. From the Clinical Pharmacology Unit, and the Department of Medicine (M.M., A.C.), University of Cambridge, United Kingdom; and NephroUrology Unit, Great Ormond Street Hospital, London, United Kingdom (W.V.H.).

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

Reference22 articles.

1. HYPERTENSION AND HYPERPOTASSÆMIA WITHOUT RENAL DISEASE IN A YOUNG MALE

2. Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21

3. Linkage of Gordon’s syndrome to the long arm of chromosome 17 in a region recently linked to familial essential hypertension

4. Genetic heterogeneity of familial hyperkalaemic hypertension

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