A shared chromosome‐21 haplotype among amyotrophic lateral sclerosis families with the A4V SOD1 mutation

Clinical GeneticsVolume 66, Issue 3 p. 247-250 A shared chromosome-21 haplotype among amyotrophic lateral sclerosis families with the A4V SOD1 mutation D R Rosen, Corresponding Author D R Rosen Daniel R. Rosen Wadsworth Center New York State Department of Health Empire State Plaza Albany NY 12201-0509 USA e-mail: [email protected]Search for more papers by this author D R Rosen, Corresponding Author D R Rosen Daniel R. Rosen Wadsworth Center New York State Department of Health Empire State Plaza Albany NY 12201-0509 USA e-mail: [email protected]Search for more papers by this author First published: 25 June 2004 https://doi.org/10.1111/j.1399-0004.2004.00298.xCitations: 9Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Tandan R, Bradley WG. Amyotrophic lateral sclerosis: Part 1. Clinical features, pathology, and ethical issues in management. Ann Neurol 1985: 18: 271–280. 2 Tandan R, Bradley WG. Amyotrophic lateral sclerosis. Part 2. Etiopathogenesis. Ann Neurol 1985: 18: 419–431. 3 Siddique T, Figlewicz DA, Pericak-Vance MA et al. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. N Engl J Med 1991: 324: 1381–1384. 4 Rosen DR, Siddique T, Patterson D et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993: 362: 59–62.DOI: 10.1038/362059a0 5 Kato S, Takikawa M, Nakashima K et al. New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes. ALS 2001: 1: 163–184. 6 Rosen DR, Bowling AC, Patterson D et al. A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis. Hum Mol Genet 1994: 3: 981–987. 7 Warren AC, McInnis MG, Blaschak J et al. Dinucleotide repeat (GT)n markers on chromosome 21. Genomics 1992: 14: 818–819. 8 Rosen DR, Sapp PC, O-Regan J et al. Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1. Hum Mol Genet 1992: 1: 547. 9 Rosen DR, Sapp P, O'Regan J et al. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers. Am J Med Genet 1994: 51: 61–69. 10 The NCBI handbook [Internet]. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information; 2002 October, January 14, 2003 release. Retrieved from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=Books Citing Literature Volume66, Issue3September 2004Pages 247-250 ReferencesRelatedInformation