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Frontotemporal Dementia Caused by CHMP2B Mutations
CHMP2B mutations are a rare cause of autosomal dominant frontotemporal dementia (FTD). The best studied example is frontotemporal dementia linked to chromosome 3 (FTD-3) which occurs in a large Danish family, with a further CHMP2B mutation identified in an unrelated Belgian familial FTD patient. The...
में बचाया:
| मुख्य लेखकों: | , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Bentham Science Publishers Ltd
2011
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3182073/ https://ncbi.nlm.nih.gov/pubmed/21222599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/156720511795563764 |
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