v1
A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population.
Identifier:nobleid.org/w1/20260515/D679D8DF
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/D679D8DF)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims