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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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| Publicado en: | Transl Neurodegener |
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| Autores principales: | , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2019
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| Materias: | |
| Acceso en línea: | 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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