References
- Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature. 1993;362:59–62.
- Abel O, Powell JF, Andersen PM, Al-Chalabi A. ALSoD: a user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics. Hum Mutat. 2012;33:1345–51.
- Liu R, Tang L, Cai B, Liu X, Ye S, Ma Y, et al. C9orf72 repeat expansions are not detected in Chinese patients with familial ALS. Amyotroph Lateral Scler Frontotemporal Degener. 2013;14:630–1.
- He J, Tang L, Benyamin B, Shah S, Hemani G, Liu R, et al. C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis. Neurobiol Aging. 2015;36:2660–1.
- Wei QQ, Zhou QQ, Chen YP, Ou RW, Cao B, Xu YQ, et al. Analysis of SOD1 mutations in a Chinese population with amyotrophic lateral sclerosis: a case-control study and literature review. Sci Rep. 2017;7:44606.
- Broom WJ, Johnson DV, Auwarter KE, Iafrate AJ, Russ C, Al-Chalabi A, et al. SOD1A4V-mediated ALS: absence of a closely linked modifier gene and origination in Asia. Neurosci Lett. 2008;430:241–5.
- Saeed M, Yang Y, Deng H, Hung W, Siddique N, Dellefave L, et al. Age and founder effect of SOD1 A4V mutation causing ALS. Neurology. 2009;72:1634–9.
- Nakano R, Sato S, Inuzuka T, Sakimura K, Mishina M, Takahashi H, et al. A novel mutation in Cu/Zn superoxide dismutase gene in Japanese familial amyotrophic lateral sclerosis. Biochem Biophys Res Commun. 1994;200:695–703.
- Baek W, Koh SH, Park JS, Kim YS, Kim HY, Kwon MJ, et al. A novel codon4 mutation (A4F) in the SOD1gene in familial amyotrophic lateral sclerosis. J Neurol Sci. 2011;306:157–9.
- Cudkowicz ME, McKenna-Yasek D, Sapp PE, Chin W, Geller B, Hayden DL, et al. Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis. Ann Neurol. 1997;41:210–21.