Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia

BACKGROUND AND PURPOSE: Hereditary spastic paraplegia (HSP) is a genetically heterogeneous group of neurodegenerative disorders that are characterized by progressive spasticity and weakness of the lower limbs. Mutations in the spastin gene (SPAST) are the most common causes of HSP, accounting for 40...

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Detalhes bibliográficos
Main Authors: Kim, Tae-Hyoung, Lee, Jae-Hyeok, Park, Young-Eun, Shin, Jin-Hong, Nam, Tai-Seung, Kim, Hyang-Sook, Jang, Ho-Jung, Semenov, Artem, Kim, Sang Jin, Kim, Dae-Seong
Formato: Artigo
Idioma:Inglês
Publicado em: Korean Neurological Association 2014
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4101104/
https://ncbi.nlm.nih.gov/pubmed/25045380
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3988/jcn.2014.10.3.257
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