Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11

BACKGROUND: Spastic paraplegia type 11 (SPG11) mutations are the most frequent cause of autosomal recessive hereditary spastic paraplegia (ARHSP). We are aiming to identify the causative mutations in SPG11 among families referred to our center with ARHSP in a Chinese population. METHODS: Targeted ne...

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Detalles Bibliográficos
Autores principales: Chen, Xueping, Liu, Jiao, Wei, Qian-Qian, Ou, Ru Wei, Cao, Bei, Yuan, Xiaoqin, Hou, Yanbing, Zhang, Lingyu, Shang, Huifang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941247/
https://www.ncbi.nlm.nih.gov/pubmed/31900114
http://dx.doi.org/10.1186/s12883-019-1593-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941247/
https://www.ncbi.nlm.nih.gov/pubmed/31900114
http://dx.doi.org/10.1186/s12883-019-1593-y

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