Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations

G. P. Chrousos, D. L. Loriaux, D. Mann, G. B. Cutler

Research output: Contribution to journalArticle

39 Scopus citations

Fingerprint Dive into the research topics of 'Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations'. Together they form a unique fingerprint.

Medicine & Life Sciences