Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement

Tarih
2013
Yazar
Hanagasi, Haşmet Ayhan
BRAS, Jose Miguel
GIBBS, Jesse Raphael
Dursun, Burcu
SINGLETON, Andrew
Rohrer, Jonathan D.
Gurunlian, Nicole
Hardy, John
Lohmann, Ebba
Emre, Murat
Gurvit, Hakan
Bilgic, Başar
GUERREIRO, Rita Joao
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Özet
Objective: To identify new genes and risk factors associated with frontotemporal dementia (FTD). Several genes and loci have been associated with different forms of FTD, but a large number of families with dementia do not harbor mutations in these genes.
Bağlantı
http://hdl.handle.net/20.500.12627/110744
https://doi.org/10.1001/jamaneurol.2013.579
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