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High frequency of SPG4 in Taiwanese families with autosomal dominant hereditary spastic paraplegia
BACKGROUND: Hereditary spastic paraplegias (HSPs) are a group of neurodegenerative diseases characterized by progressive spasticity and weakness of the lower limbs. SPG4, SPG3A and SPG31 are the three leading causes of autosomal dominant (AD) HSPs. METHODS: A total of 20 unrelated AD-HSP families we...
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| 出版年: | BMC Neurol |
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| 主要な著者: | , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4254010/ https://ncbi.nlm.nih.gov/pubmed/25421405 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-014-0216-x |
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