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CSF neurofilament light concentration is increased in presymptomatic CHMP2B mutation carriers
OBJECTIVE: A rare cause of familial frontotemporal dementia (FTD) is a mutation in the CHMP2B gene on chromosome 3 (FTD-3), described in a Danish family. Here we examine whether CSF biomarkers change in the preclinical phase of the disease. METHODS: In this cross-sectional explorative study, we anal...
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| Publicado no: | Neurology |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5772154/ https://ncbi.nlm.nih.gov/pubmed/29237796 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000004799 |
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