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Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1
Mast syndrome (SPG21) is an autosomal-recessive complicated form of hereditary spastic paraplegia characterized by dementia, thin corpus callosum, white matter abnormalities, and cerebellar and extrapyramidal signs in addition to spastic paraparesis. A nucleotide insertion resulting in premature tru...
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| Publicado no: | Neurogenetics |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5585778/ https://ncbi.nlm.nih.gov/pubmed/19184135 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-009-0172-6 |
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