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CAPN1 Variants as Cause of Hereditary Spastic Paraplegia Type 76
BACKGROUND: Autosomal recessive hereditary spastic paraplegias (HSP) are a rare group of hereditary neurodegenerative disorders characterized by spasticity with or without other symptoms. SPG11 gene is the most common cause of autosomal recessive HSP. We report a case of autosomal recessive spastic...
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| Publicado no: | Case Rep Neurol Med |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6634065/ https://ncbi.nlm.nih.gov/pubmed/31355030 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/7615605 |
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