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The CYP21A2 mutations that are in linkage disequilibrium with particular HLA‐A, ‐B, ‐DRB1 alleles/haplotypes, cause deficiency of the 21‐hydroxylase enzyme (21‐OHD) and account for the majority of congenital adrenal hyperplasia (CAH) cases. The aim of this study was to investigate those associations with the p.V282L mutation linked to the non‐classical (NC) form of CAH among Croatians. The study included...