CYP21A2 and congenital adrenal hyperplasia: The non-allelic gene conversion in the background of the concerted evolution of CYP21 paralogues is well studied in humans, because congenital adrenal hyperplasia (CAH), a frequent Mendelian disorder mostly caused by gene conversion from CYP21A1P to CYP21A2, is a focus of human geneticists [21,22].