No evidence for coding region mutations in the retinoblastoma-associated Kruppel-associated box protein gene (RBaK) causing familial hyperaldosteronism type II

So, Albertina, Jeske, Yvette W.A., Gordon, Richard D., Duffy, David, Kelemen, Livia and Stowasser, Michael (2006) No evidence for coding region mutations in the retinoblastoma-associated Kruppel-associated box protein gene (RBaK) causing familial hyperaldosteronism type II. Clinical Endocrinology, 65 6: 829-831. doi:10.1111/j.1365-2265.2006.02674.x


Author So, Albertina
Jeske, Yvette W.A.
Gordon, Richard D.
Duffy, David
Kelemen, Livia
Stowasser, Michael
Title No evidence for coding region mutations in the retinoblastoma-associated Kruppel-associated box protein gene (RBaK) causing familial hyperaldosteronism type II
Journal name Clinical Endocrinology   Check publisher's open access policy
ISSN 0300-0664
Publication date 2006-12-01
Year available 2006
Sub-type Letter to editor, brief commentary or brief communication
DOI 10.1111/j.1365-2265.2006.02674.x
Volume 65
Issue 6
Start page 829
End page 831
Total pages 3
Place of publication Oxford, U.K.
Publisher Blackwell Publishing Ltd
Language eng
Subject CX
321004 Endocrinology
730105 Endocrine organs and diseases (incl. diabetes)
1103 Clinical Sciences
110306 Endocrinology
Keyword Endocrinology
Hyperaldosteronism type II
RBaK
Q-Index Code CX
Institutional Status UQ

Document type: Journal Article
Sub-type: Letter to editor, brief commentary or brief communication
Collections: Excellence in Research Australia (ERA) - Collection
School of Medicine Publications
 
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Created: Wed, 15 Aug 2007, 20:08:49 EST