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Using Exome Sequencing to Reveal Mutations in Trem2 Presenting as a Frontotemporal Dementia-Like Syndrome Without Bone Involvement

AuthID
P-005-3JZ

Author(s)

Guerreiro, RJ

Lohmann, E

Bras, JM

Gibbs, JR

Rohrer, JD

Gurunlian, N

Dursun, B

Bilgic, B

Hanagasi, H

Gurvit, H

Emre, M

Singleton, A

Hardy, J

Document Type

Article

Year published

2013

Published

in JAMA NEUROLOGY, ISSN: 2168-6149

Volume: 70, Issue: 1, Pages: 78-84 (7)

Indexing

Wos^®

Scopus^®

Crossref^®148

Pubmed^®

Google Scholar^®

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Publication Identifiers

DOI: 10.1001/jamaneurol.2013.579

Pubmed: 23318515

Scopus: 2-s2.0-84872586508

Wos: WOS:000316800300011

Source Identifiers

ISSN: 2168-6149

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Using Exome Sequencing to Reveal Mutations in Trem2 Presenting as a Frontotemporal Dementia-Like Syndrome Without Bone Involvement

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Using Exome Sequencing to Reveal Mutations in Trem2 Presenting as a Frontotemporal Dementia-Like Syndrome Without Bone Involvement

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