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Mutation of proline 409 to arginine in the meander region of cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency

Lam, CW; Arlt, W; Chan, CK; Honour, JW; Lin, CJ; Tong, SF; Choy, KW; (2001) Mutation of proline 409 to arginine in the meander region of cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency. MOLECULAR GENETICS AND METABOLISM , 72 (3) pp. 254-259. 10.1006/mgme.2000.3134.

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Type: Article
Title: Mutation of proline 409 to arginine in the meander region of cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency
DOI: 10.1006/mgme.2000.3134
Keywords: Science & Technology, Life Sciences & Biomedicine, Endocrinology & Metabolism, Genetics & Heredity, Medicine, Research & Experimental, Research & Experimental Medicine, 17 alpha-hydroxylase deficiency, male pseudohermaphroditism, mutational analysis, CYP17 gene, cytochrome P450c17, ISOLATED 17,20-LYASE DEFICIENCY, BINDING-SITE, REDUCTASE, B(5), GENE, IDENTIFICATION, ADRENODOXIN, P450SCC, PROTEIN, CLONING
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Inst for Women's Health
URI: http://discovery.ucl.ac.uk/id/eprint/191817
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