Author:
Paradisi Irene,Ikonomu Vassiliki,Arias Sergio
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference45 articles.
1. Bird, T. D. Hereditary Ataxia Overview GeneReviews [Internet], 28 Oct 1998 (updated 5 Mar 2015) (eds Pagon, R. A., Adam, M. P., Ardinger, H. H. et al) (University of Washington, Seattle, WA, 1993–2015) Available from http://www.ncbi.nlm.nih.gov/books/NBK1138/ (accessed April 2015).
2. Rüb, U., Schöls, L., Paulson, H., Auburger, G., Kermer, P., Jen, J. C. et al. Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7. Prog. Neurobiol. 104, 38–66 (2013).
3. Ruano, L, Melo, C, Silva, M. C. & Coutinho, P. The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies. Neuroepidemiology 42, 174–183 (2014).
4. Orozco, G., Estrada, R., Perry, T. L., Arana, J., Fernández, R., González-Quevedo, A. et al. Dominantly inherited olivopontocerebellar atrophy from eastern Cuba: clinical, neuropathological, and biochemical findings. J. Neurol. Sci. 93, 37–50 (1989).
5. Jonasson, J., Juvonen, V., Sistonen, P., Ignatius, J., Johansson, D., Björck, E. J. et al. Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia. Eur. J. Hum. Genet. 8, 918–922 (2000).
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