Primary aldosteronism. Part II Differential diagnosis of primary hyperaldosteronism and pseudoaldosteronism
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.1996.tb02060.x/fullpdf
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4. Deletion within the CYP17 gene together with insertion for foreign DNA is the cause of combined complete 17α-hydroxylase/17,20 lyase deficiency in an Italian patient;Biason;Molecular Endocrinology,1992
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