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Presymptomatic studies in genetic frontotemporal dementia
Approximately 20% of patients with the neurodegenerative disorder frontotemporal dementia (FTD) have an autosomal dominant pattern of inheritance. Genetic FTD is caused by mutations in three genes in most cases (progranulin, microtubule-associated protein tau and chromosome 9 open reading frame 72)...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Masson
2013
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3878569/ https://ncbi.nlm.nih.gov/pubmed/24012408 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurol.2013.07.010 |
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