Mild cognitive impairment in novel SPG11 mutation-related sporadic hereditary spastic paraplegia with thin corpus callosum: case series

BACKGROUND: SPG11 mutation-related autosomal recessive hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) is the most common cause in complicated forms of HSP, usually presenting comprehensive mental retardation on early-onset stage preceding spastic paraplegias in childhood. However,...

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Detalles Bibliográficos
Autores principales: Li, Chuan, Yan, Qi, Duan, Feng-ju, Zhao, Chao, Zhang, Zhuo, Du, Ying, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798194/
https://www.ncbi.nlm.nih.gov/pubmed/33430805
http://dx.doi.org/10.1186/s12883-020-02040-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7798194/
https://www.ncbi.nlm.nih.gov/pubmed/33430805
http://dx.doi.org/10.1186/s12883-020-02040-4

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