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A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter.
Yamashita I, Sasaki H, Yabe I, Fukazawa T, Nogoshi S, Komeichi K, Takada A, Shiraishi K, Takiyama Y, Nishizawa M, Kaneko J, Tanaka H, Tsuji S, Tashiro K. Yamashita I, et al. Among authors: nishizawa m. Ann Neurol. 2000 Aug;48(2):156-63. doi: 10.1002/1531-8249(200008)48:2<156::aid-ana4>3.0.co;2-9. Ann Neurol. 2000. PMID: 10939565
Choreiform movements in spinocerebellar ataxia type 1.
Namekawa M, Takiyama Y, Ando Y, Sakoe K, Muramatsu SI, Fujimoto KI, Nishizawa M, Nakano I. Namekawa M, et al. Among authors: nishizawa m. J Neurol Sci. 2001 Jun 15;187(1-2):103-6. doi: 10.1016/s0022-510x(01)00527-5. J Neurol Sci. 2001. PMID: 11440752
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.
Date H, Onodera O, Tanaka H, Iwabuchi K, Uekawa K, Igarashi S, Koike R, Hiroi T, Yuasa T, Awaya Y, Sakai T, Takahashi T, Nagatomo H, Sekijima Y, Kawachi I, Takiyama Y, Nishizawa M, Fukuhara N, Saito K, Sugano S, Tsuji S. Date H, et al. Among authors: nishizawa m. Nat Genet. 2001 Oct;29(2):184-8. doi: 10.1038/ng1001-184. Nat Genet. 2001. PMID: 11586299
Identification of a SACS gene missense mutation in ARSACS.
Ogawa T, Takiyama Y, Sakoe K, Mori K, Namekawa M, Shimazaki H, Nakano I, Nishizawa M. Ogawa T, et al. Among authors: nishizawa m. Neurology. 2004 Jan 13;62(1):107-9. doi: 10.1212/01.wnl.0000099371.14478.73. Neurology. 2004. PMID: 14718708
1,169 results