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)...
| Main Authors: | , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Masson
2013
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878569/ |