Clinical Characterization of Genetically Diagnosed Cases of Spinocerebellar Ataxia Type 12 from India

https://onlinelibrary.wiley.com/page/journal/23301619/homepage/mdc312551-sup-v001_1.htm BACKGROUND: Spinocerebellar ataxia type 12 (SCA12) is a rare form of an autosomal‐dominant ataxic disorder associated with an expansion of CAG repeat length. Here, we present a large case series of patients with...

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Detalhes bibliográficos
Publicado no:Mov Disord Clin Pract
Main Authors: Choudhury, Supriyo, Chatterjee, Sayan, Chatterjee, Koustav, Banerjee, Rebecca, Humby, Jonathan, Mondal, Banashree, Anand, Sidharth S., Shubham, Shantanu, Kumar, Hrishikesh
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2017
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Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6090588/
https://ncbi.nlm.nih.gov/pubmed/30363072
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12551
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