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A rare cause of congenital adrenal hyperplasia: clinical and genetic findings and follow-up characteristics of six patients with 17-hydroxylase deficiency including two novel mutations. J Clin Res Pediatr Endocrinol 10: 206-215, 2018.","DOI":"10.4274\/jcrpe.0032"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Auchus RJ. The genetics, pathophysiology, and management of human deficiencies of P450c17. Endocrinol Metab Clin N Am 30: 101-119, 2001.","DOI":"10.1016\/S0889-8529(08)70021-5"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Katayama Y, Kado S, Wada S, et al. A case of 17 \u03b1-hydroxylase deficiency with retained menstruation. Endocr J 41: 213-218, 1994.","DOI":"10.1507\/endocrj.41.213"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Ueda Y, Usui T, Watanabe T, et al. Elevated levels of plasma immunoassayable aldosterone in a mild form of 17 alpha-hydroxylase\/17,20-lyase deficiency diagnosed at the age of 50. 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