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Molecular basis of apparent isolated 17,20-lyase deficiency: compound heterozygous mutations in the C-terminal region (Arg(496)----Cys, Gln(461)----Stop) actually cause combined 17 alpha-hydroxylase/17,20-lyase deficiency.
Yanase T, Waterman MR, Zachmann M, Winter JS, Simpson ER, Kagimoto M. Yanase T, et al. Among authors: kagimoto m. Biochim Biophys Acta. 1992 Aug 25;1139(4):275-9. doi: 10.1016/0925-4439(92)90100-2. Biochim Biophys Acta. 1992. PMID: 1515452
Structural characterization of the bovine CYP17 (17 alpha-hydroxylase) gene.
Bhasker CR, Adler BS, Dee A, John ME, Kagimoto M, Zuber MX, Ahlgren R, Wang XD, Simpson ER, Waterman MR. Bhasker CR, et al. Among authors: kagimoto m. Arch Biochem Biophys. 1989 Jun;271(2):479-87. doi: 10.1016/0003-9861(89)90298-1. Arch Biochem Biophys. 1989. PMID: 2543297
Deduced amino acid sequence of mature chicken testis ferredoxin.
Kagimoto K, McCarthy JL, Waterman MR, Kagimoto M. Kagimoto K, et al. Among authors: kagimoto m. Biochem Biophys Res Commun. 1988 Aug 30;155(1):379-83. doi: 10.1016/s0006-291x(88)81096-9. Biochem Biophys Res Commun. 1988. PMID: 3415692
43 results