A Novel Compound Heterozygous CYP17A1 Variant Causes 17α-Hydroxylase/17, 20-Lyase Deficiency.
Chen H, Yuan K, Zhang B, Jia Z, Chen C, Zhu Y, Sun Y, Zhou H, Huang W, Liang L, Yan Q, Wang C.
Chen H, et al. Among authors: yuan k.
Front Genet. 2019 Oct 22;10:996. doi: 10.3389/fgene.2019.00996. eCollection 2019.
Front Genet. 2019.
PMID: 31695722
Free PMC article.