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A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia
AIMS: Frontotemporal lobar degeneration (FTLD) is a progressive neurodegenerative disease and is the second most common form of young onset dementia after Alzheimer's disease (AD). An autosomal dominant pattern of inheritance is present in around 25–50% of FTLD cases indicating a strong genetic...
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| 發表在: | Neuropathol Appl Neurobiol |
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| Main Authors: | , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BlackWell Publishing Ltd
2014
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4260146/ https://ncbi.nlm.nih.gov/pubmed/24286341 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nan.12100 |
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