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

Abstract 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....

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Principais autores:	Chuan Li, Qi Yan, Feng-ju Duan, Chao Zhao, Zhuo Zhang, Ying Du, Wei Zhang
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2021-01-01
Colecção:	BMC Neurology
Assuntos:	SPG11 Next generation sequencing Hereditary spastic paraplegia Mild cognitive impairment
Acesso em linha:	https://doi.org/10.1186/s12883-020-02040-4
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