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Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
BACKGROUND: Spastic paraplegia type 11 (SPG11) mutations are the most frequent cause of autosomal recessive hereditary spastic paraplegia (ARHSP). We are aiming to identify the causative mutations in SPG11 among families referred to our center with ARHSP in a Chinese population. METHODS: Targeted ne...
Tallennettuna:
| Julkaisussa: | BMC Neurol |
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| Päätekijät: | , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6941247/ https://ncbi.nlm.nih.gov/pubmed/31900114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-019-1593-y |
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