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Longitudinal imaging in C9orf72 mutation carriers: Relationship to phenotype
Expansion mutations in the C9orf72 gene may cause amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), or mixtures of the two clinical phenotypes. Different imaging findings have been described for C9orf72-associated diseases in comparison with sporadic patients with the same phenotyp...
Gorde:
| Argitaratua izan da: | Neuroimage Clin |
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| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Elsevier
2016
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5153604/ https://ncbi.nlm.nih.gov/pubmed/27995069 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2016.10.014 |
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