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

dc.contributor.authorHanagasi, Haşmet Ayhan
dc.contributor.authorBRAS, Jose Miguel
dc.contributor.authorGIBBS, Jesse Raphael
dc.contributor.authorDursun, Burcu
dc.contributor.authorSINGLETON, Andrew
dc.contributor.authorRohrer, Jonathan D.
dc.contributor.authorGurunlian, Nicole
dc.contributor.authorHardy, John
dc.contributor.authorLohmann, Ebba
dc.contributor.authorEmre, Murat
dc.contributor.authorGurvit, Hakan
dc.contributor.authorBilgic, Başar
dc.contributor.authorGUERREIRO, Rita Joao
dc.date.accessioned2021-03-05T10:55:17Z
dc.date.available2021-03-05T10:55:17Z
dc.date.issued2013
dc.identifier.citationGUERREIRO R. J. , Lohmann E., BRAS J. M. , GIBBS J. R. , Rohrer J. D. , Gurunlian N., Dursun B., Bilgic B., Hanagasi H. A. , Gurvit H., et al., "Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement", JAMA NEUROLOGY, cilt.70, sa.1, ss.78-84, 2013
dc.identifier.issn2168-6149
dc.identifier.othervv_1032021
dc.identifier.otherav_a5932627-566e-43e7-9b80-7ad647b1b416
dc.identifier.urihttp://hdl.handle.net/20.500.12627/110744
dc.identifier.urihttps://doi.org/10.1001/jamaneurol.2013.579
dc.description.abstractObjective: 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.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectKLİNİK NEUROLOJİ
dc.titleUsing Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement
dc.typeMakale
dc.relation.journalJAMA NEUROLOGY
dc.contributor.departmentNational Institutes of Health (NIH) - USA , ,
dc.identifier.volume70
dc.identifier.issue1
dc.identifier.startpage78
dc.identifier.endpage84
dc.contributor.firstauthorID99066


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