SIGMAR1 mutations, genetic heterogeneity at the chromosome 9p locus, and the expanding etiological diversity of amyotrophic lateral sclerosis
Fecto, F.; Siddique, T.
Annals of Neurology 70(6): 867-870
2011
ISSN/ISBN: 1531-8249 PMID: 22190360 DOI: 10.1002/ana.22648
Accession: 055632705
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Siddique, T.; Isozumi, K. 1996: From the discovery of genetic linkage to chromosome 21 and mutations in SOD1 to the molecular basis of familial amyotrophic lateral sclerosis Nakano, I, Hirano, A International Congress Series; Amyotrophic lateral sclerosis: Progress and perspectives in basic research and clinical application 266-275
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Maekawa, S.; Leigh, P.N.; King, A.; Jones, E.; Steele, J.C.; Bodi, I.; Shaw, C.E.; Hortobagyi, T.; Al-Sarraj, S. 2009: TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations Neuropathology: Official Journal of the Japanese Society of Neuropathology 29(6): 672-683
Sako, W.; Ito, H.; Yoshida, M.; Koizumi, H.; Kamada, M.; Fujita, K.; Hashizume, Y.; Izumi, Y.; Kaji, R. 2012: Nuclear factor κ B expression in patients with sporadic amyotrophic lateral sclerosis and hereditary amyotrophic lateral sclerosis with optineurin mutations Clinical Neuropathology 31(6): 418-423
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