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Human Mutation|July 19, 2002
Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegiaS Sauter, B Miterski, S Klimpe, et al.
Neurology|July 13, 2005
Early-onset ALS with long-term survival associated with spastin gene mutationT Meyer, A Schwan, J S Dullinger, et al.
Genes and Immunity|February 24, 2001
Lack of association between the interferon regulatory factor-1 (IRF1) locus at 5q31.1 and multiple sclerosis in Germany, northern Italy, Sardinia and SwedenK Vandenbroeck, C Hardt, J Louage, et al.
American Journal of Human Genetics|June 5, 2001
Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levelsC Walter, J Gootjes, P A Mooijer, et al.
Annals of the Rheumatic Diseases|April 18, 2013
Genetics of toll like receptor 9 in ANCA associated vasculitidesC A Husmann, J U Holle, F Moosig, et al.
Neuroreport|August 3, 2000
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patientsP Wintermeyer, R Krüger, W Kuhn, et al.
Neurology|September 26, 1997
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6T Sander, B Bockenkamp, T Hildmann, et al.
Archives of Neurology|October 6, 1997
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindredsL Schöls, S Gispert, M Vorgerd, et al.
American Journal of Medical Genetics|April 17, 1999
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14T Sander, H Schulz, A M Vieira-Saeker, et al.
Annals of Neurology|May 13, 1999
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotypeR Krüger, A M Vieira-Saecker, W Kuhn, et al.
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