v1
Mutation R96W in cytochrome P450c17 gene causes combined 17 alpha-hydroxylase/17-20-lyase deficiency in two French Canadian patients.
Identifier:nobleid.org/w1/20260515/CF9207AF
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/CF9207AF)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims