v1
Novel nonsense mutation (W302X) in the steroid 21-hydroxylase gene of a Finnish patient with the salt-wasting form of congenital adrenal hyperplasia.
Identifier:nobleid.org/w1/20260515/7BF3DFC5
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/7BF3DFC5)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims