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|Title:||A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiency.|
|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.|
|Appears in Collections:||Published Articles, Dept. of Biochemistry|
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