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Frontotemporal dementia–amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1–q12.2: genetic, clinical and neuropathological analysis

Numerous families exhibiting both frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) have been described, and although many of these have been shown to harbour a repeat expansion in C9ORF72, several C9ORF72-negative FTD-ALS families remain. We performed neuropathological and genet...

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Bibliografiske detaljer
Main Authors: Dobson-Stone, Carol, Luty, Agnes A., Thompson, Elizabeth M., Blumbergs, Peter, Brooks, William S., Short, Cathy L., Field, Colin D., Panegyres, Peter K., Hecker, Jane, Solski, Jennifer A., Blair, Ian P., Fullerton, Janice M., Halliday, Glenda M., Schofield, Peter R., Kwok, John B. J.
Format: Artigo
Sprog:Inglês
Udgivet: Springer-Verlag 2013
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Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3611035/
https://ncbi.nlm.nih.gov/pubmed/23338750
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-013-1078-9
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