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Brain : a Journal of Neurology|March 1, 1997
The phenotypic manifestations of chromosome 17p11.2 duplicationP K Thomas, W Marques, M B Davis, et al.Brain : a Journal of Neurology|February 1, 1991
Neuroacanthocytosis. A clinical, haematological and pathological study of 19 casesR J Hardie, H W Pullon, A E Harding, et al.American Journal of Human Genetics|December 1, 1996
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locusG David, P Giunti, N Abbas, et al.Lancet (London, England)|June 6, 1992
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's diseaseC A Smith, A C Gough, P N Leigh, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1995
Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studiesS P Morrissey, F X Borruat, D H Miller, et al.Journal of the Neurological Sciences|January 1, 1994
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsyM G Sweeney, S R Hammans, L W Duchen, et al.Annals of Neurology|July 1, 1996
Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.Annals of Neurology|October 1, 1996
Exclusion of the DYT1 locus in familial torticollisS B Bressman, T T Warner, L Almasy, et al.Pageof 21