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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101104/
https://www.ncbi.nlm.nih.gov/pubmed/25045380
http://dx.doi.org/10.3988/jcn.2014.10.3.257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101104/
https://www.ncbi.nlm.nih.gov/pubmed/25045380
http://dx.doi.org/10.3988/jcn.2014.10.3.257

Ejemplares similares