A rare intronic mutation in the splice acceptor site of the CYP17A1 gene in a patient with 17α-hydroxylase/17,20-lyase deficiency
Guo, Xudong, Wang, Hanbo, Xiang, Yuzhu, Ren, Xiangbin, Jiang, ShaoboJournal:
Gynecological Endocrinology
DOI:
10.1080/09513590.2020.1822799
Date:
September, 2020
File:
PDF, 1002 KB
2020