A comprehensive assessment of benign genetic variability for neurodegenerative disorders
Over the last few years, as more and more sequencing studies have been performed, it has become apparent that the identification of pathogenic mutations is, more often than not, a complex issue. Here, with a focus on neurodegenerative diseases, we have performed a survey of coding genetic variabilit...
| Main Authors: | Guerreiro, Rita, Sassi, Celeste, Gibbs, Jesse, Edsall, Connor, Hernandez, Dena, Brown, Kristelle, Lupton, Michelle, Parkinnen, Laura, Ansorge, Olaf, Hodges, Angela, Ryten, Mina, Tienari, Pentti, Van Deerlin, Vivanna, Trojanowski, John, Morgan, Kevin, Powell, John, Singleton, Andrew, Hardy, John, Bras, Jose |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
2018
|
| Online Access: | https://eprints.nottingham.ac.uk/50595/ |
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