1. A novel homozygous CYP17A1 mutation causes partial 17 α-hydroxylase/17, 20-lyase deficiency in 46, XX: a case report and literature review. (31st December 2023) Authors: Chen, Heye; Chen, Yingting; Mao, Hongxian; Huang, Huaying; Lou, Xueyong Journal: Blood pressure Issue: Volume 32:Number 1(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗