A rare CYP 21 mutation (p. E431K) induced deactivation of CYP 21A2 and resulted in congenital adrenal hyperplasia
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Target Article[edit | edit source]
A rare CYP 21 mutation (p. E431K) induced deactivation of CYP 21A2 and resulted in congenital adrenal hyperplasia; Y Kawashima, T Usui, M Fujimoto, N Miyaharaae; 2014; 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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