Inter-generational instability of inserted repeats during transmission in spinocerebellar ataxia type 31
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/jhg201763.pdf
Reference16 articles.
1. Ouyang, Y., Sakoe, K., Shimazaki, H., Namekawa, M., Ogawa, T., Ando, Y. et al. 16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study. J. Neurol. Sci. 247, 180–186 (2006).
2. Onodera, Y., Aoki, M., Mizuno, H., Warita, H., Shiga, Y. & Itoyama, Y. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese. Neurology 67, 1300–1302 (2006).
3. Nozaki, H., Ikeuchi, T., Kawakami, A., Kimura, A., Koide, R., Tsuchiya, M. et al. Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population. Mov. Disord. 22, 857–862 (2007).
4. Basri, R., Yabe, I., Soma, H. & Sasaki, H. Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families. J. Hum. Genet. 52, 848–855 (2007).
5. Hayashi, M., Adachi, Y., Mori, M., Nakano, T. & Nakashima, K. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan. Acta Neurol. Scand. 116, 123–127 (2007).
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