A proteomic network approach across the ALS‐FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brain

Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are neurodegenerative diseases with overlap in clinical presentation, neuropathology, and genetic underpinnings. The molecular basis for the overlap of these disorders is not well established. We performed a comparative unbiased m...

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Detalles Bibliográficos
Autores principales: Umoh, Mfon E, Dammer, Eric B, Dai, Jingting, Duong, Duc M, Lah, James J, Levey, Allan I, Gearing, Marla, Glass, Jonathan D, Seyfried, Nicholas T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760858/
https://www.ncbi.nlm.nih.gov/pubmed/29191947
http://dx.doi.org/10.15252/emmm.201708202

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760858/
https://www.ncbi.nlm.nih.gov/pubmed/29191947
http://dx.doi.org/10.15252/emmm.201708202

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