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A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disorders

Mutations in the TANK-binding kinase 1 (TBK1) gene have recently been shown to cause frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). The phenotype is highly variable and has been associated with behavioral variant FTD, primary progressive aphasia, and pure ALS. We describe the...

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Foilsithe in:Cold Spring Harb Mol Case Stud
Main Authors: Lamb, Ruth, Rohrer, Jonathan D., Real, Raquel, Lubbe, Steven J., Waite, Adrian J., Blake, Derek J., Walters, R. Jon, Lashley, Tammaryn, Revesz, Tamas, Holton, Janice L., Morris, Huw R.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Cold Spring Harbor Laboratory Press 2019
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6549548/
https://ncbi.nlm.nih.gov/pubmed/31160356
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/mcs.a003913
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