Exome sequencing identifies three novel AD‐associated genes

Background With the development of next‐generation sequencing technologies, it is possible to identify rare genetic variants that influence the risk of complex disorders. To date, whole exome sequencing (WES) strategies have shown that specific clusters of damaging rare variants in the TREM2, SORL1...

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Veröffentlicht in:	Alzheimer's & dementia 2020-12, Vol.16, p.n/a
Hauptverfasser:	Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier‐Boley, Benjamin, Quenez, Olivier, Ahmad, Shahzad, Amin, Najaf, van Rooij, Jeroen G.J., Grozeva, Detelina, Norsworthy, Penny, Hummerich, Holger, Kawalia, Amit, Mok, Kin Y., Shoai, Maryam, Dols‐Icardo, Oriol, van Der Flier, Wiesje, Sims, Rebecca, Amouyel, Philippe, Hardy, John, Clarimon, Jordi, Mead, Simon, van Swieten, John C., Ramirez, Alfredo, van Duijn, Cornelia M., Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean‐Charles
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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