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From neurodevelopment to neurodegeneration: the interaction of neurofibromin and valosin-containing protein/p97 in regulation of dendritic spine formation
Both Neurofibromatosis type I (NF1) and inclusion body myopathy with Paget's disease of bone and frontotemporal dementia (IBMPFD) are autosomal dominant genetic disorders. These two diseases are fully penetrant but with high heterogeneity in phenotypes, suggesting the involvement of genetic mod...
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2012
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| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3326706/ https://ncbi.nlm.nih.gov/pubmed/22449146 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1423-0127-19-33 |
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