Amyotrophic Lateral Sclerosis and Spinocerebellar Ataxia Type 2 in a Family with Full CAG Repeat Expansions of ATXN2

IMPORTANCE: To report a family with coexistence of spinocerebellar ataxia type 2 (SCA2) and amyotrophic lateral sclerosis (ALS). OBSERVATIONS: The intermediate or full CAG repeat expansions of ATXN2 are associated with ALS. However, no coexistence of SCA2 and ALS in a family has been reported in the...

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Detalhes bibliográficos
Main Authors: Tazen, Sirinan, Figueroa, Karla, Kwan, Justin Y, Goldman, Jill, Hunt, Ann, Sampson, Jacinda, Gutmann, Laurie, Pulst, Stefan, Mitsumoto, Hiroshi, Kuo, Sheng-Han
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4039635/
https://ncbi.nlm.nih.gov/pubmed/23959108
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamaneurol.2013.443
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