A Comparative Optical Coherence Tomography Study of Spinocerebellar Ataxia Types 3 and 10
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/article/10.1007/s12311-017-0856-7/fulltext.html
Reference28 articles.
1. Teive HAG, Ashizawa T. Primary and secondary ataxias. Curr Opin Neurol. 2015;28:413–22.
2. Pestronk A. Hereditary ataxies: dominant. Washington University in Saint Louis (2016). at < http://neuromuscular.wustl.edu/ataxia/domatax.html>
3. Cintra VP, et al. Mutational screening of 320 Brazilian patients with autosomal dominant spinocerebellar ataxia. J Neurol Sci. 2014;347:375–9.
4. Teive HAG, et al. Spinocerebellar ataxias—genotype-phenotype correlations in 104 Brazilian families. Clinics. 2012;67:443–9.
5. Freund AA, et al. Spinocerebellar ataxias: microsatellite and allele frequency in unaffected and affected individuals. Arq Neuropsiquiatr. 2009;67:1124–32.
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