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Parkinsonian Syndrome in Familial Frontotemporal Dementia
Parkinsonism in frontotemporal dementia (FTD) was first described in families with mutations in the microtubule-associated protein tau (MAPT) and progranulin (PRGN) genes. Since then, mutations in several other genes have been identified for FTD with Parkinsonism, including chromosome 9 open reading...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4160731/ https://ncbi.nlm.nih.gov/pubmed/24998994 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2014.06.004 |
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