Author:
Kagimoto Keiko,Waterman Michael R.,Kagimoto Masaaki,Ferreira P.,Simpson Evan R.,Winter Jeremy S. D.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference7 articles.
1. Biglieri EG, Herron MA, Brust N (1966) 17-Hydroxylation deficiency in man. J Clin Invest 45:1946?1954
2. Dean HJ, Shackleton CHL, Winter JSD (1984) Diagnosis and natural history of 17-hydroxylase deficiency in a newborn male. J Clin Endocrinol Metab 59:513?520
3. Kagimoto M, Winter JSD, Kagimoto K, Simpson ER, Waterman MR (1988) Structural characterization of normal and mutant human steroid 17?-hydroxylase genes: molecular basis of one example of combined 17?-hydroxylase/17,20-lyase deficiency. Mol Endocrinol 2:564?570
4. Nebert DW, Nelson DR, Adesnik M, Coon MJ, Estabrook RW, Gonzalez FJ, Guengerich FP, Gunsalus IC, Johnson EF, Kemper B, Levin W, Phillips IR, Sato R, Waterman MR (1989) The P450 superfamily: update on listing of all genes and recommended nomenclature of the chromosomal loci. DNA 8:1?13
5. New MI, DuPont B, Grumbach K, Levine LS (1983) Congenital adrenal hyperplasia and related conditions. In: Stanbury JB, Wyngarden JB, Fredrickson DS, Goldstein JL, Brown MS (eds) The metabolic basis of inherited disease. McGraw-Hill, New York, pp 973?1000
Cited by
51 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献