In vitro functional studies of rare CYP 21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia

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Bibliographic Details
Published in:Clinical endocrinology (Oxford) 2015-01, Vol.82 (1), p.37-44
Main Authors: Barbaro, Michela, Soardi, Fernanda C., Östberg, Linus J., Persson, Bengt, de Mello, Maricilda Palandi, Wedell, Anna, Lajic, Svetlana
Format: Article
Language:English
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ISSN:0300-0664
1365-2265
DOI:10.1111/cen.12526