Search for a Founder Mutation in Idiopathic Focal Dystonia from Northern Germany

This publication has 26 references indexed in Scilit:

• Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family
  Movement Disorders, 1997
• The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein
  Nature Genetics, 1997
• Sporadic focal dystonia in Northwest Germany: Molecular basis on chromosome 18p
  Annals of Neurology, 1997
• Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
  Science, 1997
• Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution
  Human Molecular Genetics, 1996
• Exclusion of the DYT1 locus in familial torticollis
  Annals of Neurology, 1996
• A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
  Nature Genetics, 1996
• Adult onset idiopathic torsion dystonia is excluded from the DYT 1 region (9q34) in a Swedish family.
  Journal of Neurology, Neurosurgery & Psychiatry, 1995
• Dystonia in Ashkenazi Jews: Clinical characterization of a founder mutation
  Annals of Neurology, 1994
• A rapid and non‐radioactive PCR based assay for the detection of allelic loss in human gliomas
  Neuropathology and Applied Neurobiology, 1993