Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia

BACKGROUND: Although many causative genes of hereditary spastic paraplegia (HSP) have been uncovered in recent years, there are still approximately 50% of HSP patients without genetically diagnosis, especially in autosomal recessive (AR) HSP patients. Rare studies have been performed to determine th...

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Vydáno v:Transl Neurodegener
Hlavní autoři: Wei, Qiao, Dong, Hai-Lin, Pan, Li-Ying, Chen, Cong-Xin, Yan, Yang-Tian, Wang, Rou-Min, Li, Hong-Fu, Liu, Zhi-Jun, Tao, Qing-Qing, Wu, Zhi-Ying
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2019
Témata:
Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6593507/
https://ncbi.nlm.nih.gov/pubmed/31289639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40035-019-0157-9
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