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[Analysis of CYP17A1 gene mutation in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficiency].
|Title||[Analysis of CYP17A1 gene mutation in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficiency].|
|Publication Type||Journal Article|
|Year of Publication||2013|
|Authors||Yang K, Zhang B, Cui S-xian, Guo Q-nan, Hou Q-fang, Li Q-cheng, Liao S-xiu|
|Journal||Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics|
|Date Published||2013 Aug|
To analyze CYP17A1 gene mutations in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficiency (17OHD), and to review characteristics of CYP17A1 gene mutations in Chinese patients with 17OHD.
|Alternate Journal||Zhonghua Yi Xue Yi Chuan Xue Za Zhi|