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

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/JPEM.2000.13.6.663

Citation piece

Note: Open to append information.