TY  - GEN
AU  - van den Heuvel,L P
AU  - Luiten,B
AU  - Smeitink,J A
AU  - de Rijk-van Andel,J F
AU  - Hyland,K
AU  - Steenbergen-Spanjers,G C
AU  - Janssen,R J
AU  - Wevers,R A
TI  - A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population
SN  - 0340-6717
PY  - 1998///0818
KW  - Chromosomes, Human, Pair 11
KW  - Denmark
KW  - Dystonia
KW  - drug therapy
KW  - Genes, Recessive
KW  - Humans
KW  - Levodopa
KW  - therapeutic use
KW  - Point Mutation
KW  - Polymorphism, Single-Stranded Conformational
KW  - Tyrosine 3-Monooxygenase
KW  - genetics
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1007/s004390050756
ER  -