Associated Papers
A Novel Compound Heterozygous CYP17A1 Variant Causes 17α-Hydroxylase/17, 20-Lyase Deficiency.
Chen H et al.
Frontiers in Genetics, 2019
A novel compound heterozygous mutation in the CYP17A1 gene in a patient with 17α-hydroxylase/17,20-lyase deficiency.
Sun M et al.
Discovery Medicine, 2017
[Genetic mutation analysis of a kindred with a patient suffering from 17 alpha-hydroxylase/17, 20-lyase deficiency].
Chen Y et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics, 2009
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