A human β-III-spectrin spinocerebellar ataxia type 5 mutation causes high-affinity F-actin binding
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep21375.pdf
Reference37 articles.
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3. Stevanin, G., Herman, A., Brice, A. & Durr, A. Clinical and MRI findings in spinocerebellar ataxia type 5. Neurology 53, 1355–1357 (1999).
4. Burk, K. et al. Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred. Neurology 62, 327–329 (2004).
5. Jacob, F. D., Ho, E. S., Martinez-Ojeda, M., Darras, B. T. & Khwaja, O. S. Case of infantile onset spinocerebellar ataxia type 5. J Child Neurol 28, 1292–1295 (2013).
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