The frequency of eight common point mutations in CYP21 gene in Iranian patients with congenital adrenal hyperplasia: Revision history

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    11 August 2022

    • curprev 22:1322:13, 11 August 2022‎ 187.21.138.9 talk‎ 546 bytes +546‎ Created page with "== Target Article == The frequency of eight common point mutations in CYP21 gene in Iranian patients with congenital adrenal hyperplasia; A amazani, K Kahrizi, M azaghiazarae; 2008; doi_citing_unknown == Retraction == Bilateral ovarian steroid cell tumor in congenital adrenal hyperplasia due to classic 11ß-hydroxylase deficiency ; Firdevs Bas Nucin Saka Feyza Darendeliler Siki Tuzlah Ridvan Ilhan Ruveyde Bundak Hulya Gonuz; 06/01/2000 ; https://doi.org/0.1515/JP..."
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