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Mutation of Proline 409 to Arginine in the Meander Region of Cytochrome P450c17 Causes Severe 17α-Hydroxylase Deficiency

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Year: 2001
Type: article
Source: Molecular Genetics and Metabolism
DOI: 10.1006/mgme.2000.3134
Authors: Ching-Wan Lam, Wiebke Arlt, Chi-Kwok Chan, John W. Honour, Chin Jia Lin, Sui-Fan Tong, Kwong-Wai Choy, Walter L. Miller
Institutions: Chinese University of Hong Kong, Prince of Wales Hospital, University of California, San Francisco, University College London
Language: English

Topic: Sexual Differentiation and Disorders
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institute of Diabetes and Digestive and Kidney Diseases, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G1012478671, G1894500483
OpenAlex ID: W2009171567
FWCI: 1.086
Cites: 34
Cited by: 65
Related to: 10
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