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bibliographicCitation Müssig K, Kaltenbach S, Machicao F, Maser-Gluth C, Hartmann MF, Wudy SA, Schnauder G, Häring H, Seif FJ, Gallwitz B. 17α-Hydroxylase/17,20-Lyase Deficiency Caused by a Novel Homozygous Mutation (Y27Stop) in the Cytochrome CYP17 Gene. The Journal of Clinical Endocrinology & Metabolism. 2005 Jul;90(7):4362–5. doi: 10.1210/jc.2005-0136.
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title 17alpha-hydroxylase/17,20-lyase deficiency caused by a novel homozygous mutation (Y27Stop) in the cytochrome CYP17 gene
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