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

✍ Scribed by 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 ;Singleton, Andrew ;Hardy, John


Book ID
118158456
Publisher
American Medical Association
Year
2012
Tongue
English
Weight
498 KB
Category
Article
ISSN
2168-6149

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