Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement.

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Published in JAMA Neurol on January 01, 2013

Authors

Rita João Guerreiro1, Ebba Lohmann, José Miguel Brás, Jesse Raphael Gibbs, Jonathan D Rohrer, Nicole Gurunlian, Burcu Dursun, Basar Bilgic, Hasmet Hanagasi, Hakan Gurvit, Murat Emre, Andrew Singleton, John Hardy

Author Affiliations

1: Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA. r.guerreiro@ucl.ac.uk

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