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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 |
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| Main Authors: | , , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Cold Spring Harbor Laboratory Press
2019
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| 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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