Clinical and Genetic Characteristics of 17 α-Hydroxylase/17, 20-Lyase Deficiency: c.985_987delTACinsAA Mutation of CYP17A1 Prevalent in the Chinese Han Population
- 1 February 2021
- journal article
- research article
- Published by Elsevier BV in Endocrine Practice
- Vol. 27 (2), 137-145
- https://doi.org/10.4158/ep-2020-0478
Abstract
No abstract availableKeywords
Funding Information
- National Key Research and Development Program of China
- Ministry of Science and Technology of the People's Republic of China (2018YFC1002203)
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