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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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Bibliografiske detaljer
Udgivet i:BMC Neurol
Main Authors: Chen, Xueping, Liu, Jiao, Wei, Qian-Qian, Ou, Ru Wei, Cao, Bei, Yuan, Xiaoqin, Hou, Yanbing, Zhang, Lingyu, Shang, Huifang
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2020
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6941247/
https://ncbi.nlm.nih.gov/pubmed/31900114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-019-1593-y
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