The genetic and functional basis of isolated 17,20–lyase deficiency

Author:

Geller David H.,Auchus Richard J.,Mendonça Berenice B.,Miller Walter L.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference31 articles.

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2. Miller, W.L. & Tyrrell, J.B. The adrenal cortex. In Endocrinology and Metabolism, 3rd ed. (eds Felig, P., Baxter, J. & Frohman, L.) 555–717 (McGraw-Hill, New York, (1995).

3. Zachman, M., Vollmin, J.A., Hamilton, W. & Prader, A. Steroid 17,20-desmolase deficiency: a new cause of male pseudohermaphroditism. Clin. Endocrinol. 1, 369–385 (1972).

4. Yanase, T., Simpson, E.R. & Waterman, M.R. 17α-hydroxylase/17,20-lyase deficiency: from clinical investigation to molecular definition. Endocr. Rev. 12, 91–108 (1991).

5. Nakajin, S., Shively, J.E., Yuan, P. & Hall, P.F. Microsomal cytochrome P450 from neonatal pig testis: two enzymatic activities (17α-hydroxylase and C17,20-lyase) associated with one protein. Biochemistry 20, 4037–4042 (1981).

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