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Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement
Guerreiro, Rita João, Lohmann, Ebba, Brás, José Miguel, Gibbs, Jesse Raphael, Rohrer, Jonathan D., Gurunlian, Nicole, Dursun, Burcu, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat, SingleVolume:
70
Langue:
english
Journal:
JAMA Neurology
DOI:
10.1001/jamaneurol.2013.579
Date:
January, 2013
Fichier:
PDF, 504 KB
english, 2013