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Aged Tmem106b knockout mice display gait deficits in coincidence with Purkinje cell loss and only limited signs of non‐motor dysfunction

Genetic variants in TMEM106B are a major risk factor for several neurodegenerative diseases including frontotemporal degeneration, limbic‐predominant age‐related TDP‐43 encephalopathy, Parkinson's disease, late‐onset‐Alzheimer's disease and constitute a genetic determinant of differential...

詳細記述

保存先:
書誌詳細
出版年:Brain Pathol
主要な著者: Stroobants, Stijn, D’Hooge, Rudi, Damme, Markus
フォーマット: Artigo
言語:Inglês
出版事項: John Wiley and Sons Inc. 2020
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC8018119/
https://ncbi.nlm.nih.gov/pubmed/33016371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bpa.12903
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