A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family()

Triggering receptor expressed on myeloid cells 2 (TREM2) homozygous mutations cause Nasu-Hakola disease, an early-onset recessive form of dementia preceded by bone cysts and fractures. The same type of mutations has recently been shown to cause frontotemporal dementia (FTD) without the presence of a...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Guerreiro, Rita, Bilgic, Basar, Guven, Gamze, Brás, José, Rohrer, Jonathan, Lohmann, Ebba, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat
Natura: Artigo
Lingua:Inglês
Pubblicazione: Elsevier 2013
Soggetti:
Genetic Reports Abstract
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3898264/
https://ncbi.nlm.nih.gov/pubmed/23870839
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2013.06.005
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi