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Progranulin and TMEM106B: when two become wan
Mutations in GRN, which encodes progranulin, are a common cause of familial frontotemporal dementia (FTD). FTD is a devastating disease characterised by neuronal loss in the frontal and temporal lobes that leads to changes in personality, behaviour and language. There are no effective treatments for...
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| Pubblicato in: | EMBO Rep |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7534635/ https://ncbi.nlm.nih.gov/pubmed/32985120 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/embr.202051668 |
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