A mutation (pro-30 to leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

Maria Teresa Tusie-Luna, Phyllis W. Speiser, Miro Dumic, Maria I. New, Perrin C. White

Research output: Contribution to journalArticlepeer-review

161 Scopus citations

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Medicine & Life Sciences