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Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion
Hexanucleotide repeat expansion in C9orf72 represents the most common genetic cause of familial and sporadic behavioural variant frontotemporal dementia. Previous studies show that some C9orf72 carriers with behavioural variant frontotemporal dementia exhibit distinctive atrophy patterns whereas oth...
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| Autors principals: | , , , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4208465/ https://ncbi.nlm.nih.gov/pubmed/25273996 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awu248 |
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