A Proposal for Classification of Retinal Degeneration in Spinocerebellar Ataxia Type 7
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1007/s12311-020-01215-6.pdf
Reference38 articles.
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2. Martin JJ. Spinocerebellar ataxia type 7. In: Subramony SH, Durr A, editors. Handbook of clinical neurology, vol. 103; 2012. p. 475–91.
3. Albuquerque MVC, Pedroso JL, Braga-Neto P, Barsottini OG. Phenotype and early onset ataxia symptoms in spinocerebellar ataxia type 7: comparison and correlation with other spinocerebellar ataxias. Arq Neuropsiquiatr. 2015;73(1):18–21.
4. David G, Durr A, Stevanin G, et al. Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA 7). Hum Mol Genet. 1998;7(2):165–70.
5. Aleman TS, Cideciyan AV, Volpe NJ, Stevanin G, Brice A, Jacobson SG. Spinocerebellar ataxia type 7 shows a cone-rod dystrophy phenotype. Exp Eye Res. 2002;74(6):737–45.
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