A p. P30L mutation at the CYP21A2 gene in Macedonian patients with nonclassical congenital adrenal hyperplasia
Revision as of 00:05, 12 August 2022 by 187.21.138.9 (talk) (Created page with "== Target Article == A p. P30L mutation at the CYP21A2 gene in Macedonian patients with nonclassical congenital adrenal hyperplasia; V Anastasovska, E Kocova, M Kocova; 2010; 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/JPEM.2000...")
Target Article[edit | edit source]
A p. P30L mutation at the CYP21A2 gene in Macedonian patients with nonclassical congenital adrenal hyperplasia; V Anastasovska, E Kocova, M Kocova; 2010; doi_citing_unknown
Retraction[edit | edit source]
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
Citation piece[edit | edit source]
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