A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegia

BACKGROUND: Hereditary spastic paraplegia is a heterogeneous group of clinically and genetically neurodegenerative diseases characterized by progressive gait disorder. Hereditary spastic paraplegia can be inherited in various ways, and all modes of inheritance are associated with multiple genes or l...

Descripción completa

Detalles Bibliográficos
Autores principales: Yu, Weiwei, Jin, Haiqiang, Deng, Jianwen, Nan, Ding, Huang, Yining
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268315/
https://www.ncbi.nlm.nih.gov/pubmed/32493220
http://dx.doi.org/10.1186/s12881-020-01053-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268315/
https://www.ncbi.nlm.nih.gov/pubmed/32493220
http://dx.doi.org/10.1186/s12881-020-01053-7

Ejemplares similares