Novel ATL1 mutation in a Chinese family with hereditary spastic paraplegia: A case report and review of literature

BACKGROUND: Hereditary spastic paraplegias (HSPs) refer to a group of heterogeneous neurodegenerative diseases characterized by lower limbs spasticity and weakness. So far, over 72 genes have been found to cause HSP (SPG1-SPG72). Among autosomal dominant HSP patients, spastic paraplegia 4 (SPG4/SPAS...

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Detalles Bibliográficos
Autores principales: Xiao, Xue-Wen, Du, Juan, Jiao, Bin, Liao, Xin-Xin, Zhou, Lu, Liu, Xi-Xi, Yuan, Zhen-Hua, Guo, Li-Na, Wang, Xin, Shen, Lu, Lin, Zhang-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580333/
https://www.ncbi.nlm.nih.gov/pubmed/31236401
http://dx.doi.org/10.12998/wjcc.v7.i11.1358

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580333/
https://www.ncbi.nlm.nih.gov/pubmed/31236401
http://dx.doi.org/10.12998/wjcc.v7.i11.1358

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