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The Journal of Biological Chemistry|December 5, 1990
Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virusM T Tusie-Luna, P Traktman, P C WhiteMolecular Endocrinology (Baltimore, Md.)|December 1, 1990
Expression of 11 beta-hydroxysteroid dehydrogenase using recombinant vaccinia virusA K Agarwal, M T Tusie-Luna, C Monder, et al.Human Mutation|January 1, 1994
Mutations in steroid 21-hydroxylase (CYP21)P C White, M T Tusie-Luna, M I New, et al.Molecular Endocrinology (Baltimore, Md.)|August 1, 1992
R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversionsA Helmberg, M T Tusie-Luna, M Tabarelli, et al.Molecular Endocrinology (Baltimore, Md.)|May 1, 1991
A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency alleleM T Tusie-Luna, P W Speiser, M Dumic, et al.Molecular Endocrinology (Baltimore, Md.)|October 1, 1991
The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortexK M Curnow, M T Tusie-Luna, L Pascoe, et al.The Journal of Clinical Investigation|August 1, 1992
Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiencyP W Speiser, J Dupont, D Zhu, et al.Pageof 1