लोड हो रहा है...
Systematic validation of variants of unknown significance in APP, PSEN1 and PSEN2
Alzheimer’s disease (AD) is a neurodegenerative disease that is clinically characterized by progressive cognitive decline. More than 200 pathogenic mutations have been identified in amyloid-β precursor protein (APP), presenilin 1 (PSEN1) and presenilin 2 (PSEN2). Additionally, common and rare varian...
में बचाया:
| में प्रकाशित: | Neurobiol Dis |
|---|---|
| मुख्य लेखकों: | , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
2020
|
| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7236786/ https://ncbi.nlm.nih.gov/pubmed/32087291 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2020.104817 |
| टैग : |
टैग जोड़ें
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!
|