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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: yabe i. 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
Twenty CAG repeats are sufficient to cause the SCA6 phenotype.
Komeichi K, Sasaki H, Yabe I, Yamashita I, Kikuchi S, Tashiro K. Komeichi K, et al. Among authors: yabe i. J Med Genet. 2001 Nov;38(11):E38. doi: 10.1136/jmg.38.11.e38. J Med Genet. 2001. PMID: 11694552 Free PMC article. No abstract available.
278 results