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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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Autors principals: 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
Idioma:Inglês
Publicat: Springer-Verlag 2013
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Accés en línia: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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