v1
Mutations of the phenylalanine hydroxylase gene in mild hyperphenylalaninemia: a novel mutation in exon 3.
Identifier:nobleid.org/w1/20260515/C90ABCF6
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/C90ABCF6)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims