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Title: A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiency.
Authors: Løvås, K
McFarlane, I
Nguyen, HH
Curran, S
Schwabe, J
Halsall, D
Bernhardt, R
Wallace, AM
Chatterjee, VK
First Published: Mar-2009
Citation: J CLIN ENDOCRINOL METAB, 2009, 94 (3), pp. 914-919
Abstract: Three siblings of Pakistani origin presented neonatally with isolated hyperreninemic hypoaldosteronism and were well controlled on fludrocortisone therapy during childhood and adolescence.
DOI Link: 10.1210/jc.2008-1524
eISSN: 1945-7197
Type: Journal Article
Appears in Collections:Published Articles, Dept. of Biochemistry

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