A novel point mutation in the GTP cyclohydrolase I gene in a Spanish family with hereditary progressive and dopa responsive dystonia
J Neurol Neurosurg Psychiatry
.
1997 Apr;62(4):420-1.
doi: 10.1136/jnnp.62.4.420.
Authors
K Beyer
,
J I Lao-Villadóniga
,
B Vecino-Bilbao
,
R Cacabelos
,
R De la Fuente-Fernández
PMID:
9120469
PMCID:
PMC1074112
DOI:
10.1136/jnnp.62.4.420
No abstract available
Publication types
Clinical Trial
Controlled Clinical Trial
Letter
MeSH terms
Dystonia / genetics*
GTP Cyclohydrolase / genetics*
Humans
Nucleotide Mapping
Pedigree
Point Mutation*
Substances
GTP Cyclohydrolase