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A case report of SPG11 mutations in a Chinese ARHSP-TCC family
BACKGROUND: Autosomal recessive hereditary spastic paraplegia (ARHSP) with thin corpus callosum (TCC) is a complicated form of hereditary spastic paraplegia, characterized by progressive spastic paraplegia, weakness of the lower extremities and is usually accompanied by mental retardation. Mutations...
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| Publicado no: | BMC Neurol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4891852/ https://ncbi.nlm.nih.gov/pubmed/27256065 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-016-0604-5 |
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