Ontology highlight
ABSTRACT:
SUBMITTER: Wider C
PROVIDER: S-EPMC2732187 | biostudies-literature | 2009 Oct
REPOSITORIES: biostudies-literature
Wider Christian C Lincoln Sarah S Dachsel Justus C JC Kapatos Gregory G Heckman Michael G MG Diehl Nancy N NN Papapetropoulos Spiridon S Mash Deborah D Rajput Alex A Rajput Ali H AH Dickson Dennis W DW Wszolek Zbigniew K ZK Farrer Matthew J MJ
Neuroscience letters 20090630 1
Dopa-responsive dystonia (DRD) is a familial childhood-onset disease characterized by fluctuating dystonia, associated with tremor and parkinsonism in some patients. In most families the disease displays autosomal dominant inheritance due to mutations in the GTP cyclohydrolase 1 gene (GCH1). Penetrance and symptom severity display strong female predominance for which gender-specific GCH1 expression has been hypothesized. In this study, GCH1 mRNA expression was measured in cerebellar tissue from ...[more]