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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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| Main Authors: | , , , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2014
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| Assuntos: | |
| Acesso em linha: | 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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