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- W2095165692 abstract "Annals of NeurologyVolume 52, Issue 6 p. 857-858 Letters The relationship of SMN to amyotrophic lateral sclerosis Thomas O. Crawford MD, Thomas O. Crawford MD Department of Neurology, Johns Hopkins University, Baltimore, MDSearch for more papers by this authorRichard L. Skolasky Jr. MA, Richard L. Skolasky Jr. MA Department of Neurology, Johns Hopkins University, Baltimore, MDSearch for more papers by this author Thomas O. Crawford MD, Thomas O. Crawford MD Department of Neurology, Johns Hopkins University, Baltimore, MDSearch for more papers by this authorRichard L. Skolasky Jr. MA, Richard L. Skolasky Jr. MA Department of Neurology, Johns Hopkins University, Baltimore, MDSearch for more papers by this author First published: 22 November 2002 https://doi.org/10.1002/ana.10378Citations: 5Read 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 References 1 Corcia P, Mayeux-Portas V, Khoris J, et al. Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis. Ann Neurol 2002; 51: 243– 246. 2 Moulard B, Salachas F, Chassande B, et al. Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron disease. Ann Neurol 1998; 43: 640– 644. 3 Lefebvre S, Bürglen L, Reboullet S, et al. Identification and characterization of a spinal muscular atrophy-determining gene. Cell 1995; 80: 155– 165. 4 Rodrigues NR, Owen N, Talbot K, et al. Gene deletions in spinal muscular atrophy. J Med Genet 1996; 33: 93– 96. 5 Mailman MD, Heinz JW, Papp AC, et al. Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2. Genet Med 2002; 4: 20– 26. 6 Jackson M, Morrison KE, Al-Chalabi A, et al. Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: homozygous NAIP deletion in a sporadic case. Ann Neurol 1996; 39: 796– 800. 7 Veldink JH, van den Berg LH, Cobben JM, et al. Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS. Neurology 2001; 56: 749– 753. 8 Kunst CB, Messer L, Gordon J, et al. Genetic mapping of a mouse modifier mene that can prevent ALS onset. Genomics 2000; 70: 181– 189. 9 Parboosingh JS, Meininger V, McKenna-Yasek D, et al. A. Deletions causing spinal muscular atrophy do not predispose to amyotrophic lateral sclerosis. Arch Neurol 1999; 56: 710– 712. Citing Literature Volume52, Issue6December 2002Pages 857-858 ReferencesRelatedInformation" @default.
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- W2095165692 title "The relationship ofSMN to amyotrophic lateral sclerosis" @default.
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