Coding variants in TREM2 increase risk for Alzheimer's disease-Reference-Cited by-同舟云学术

Coding variants in TREM2 increase risk for Alzheimer's disease

Published:2014-06-04 Issue:21 Volume:23 Page:5838-5846
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Jin Sheng Chih,Benitez Bruno A.,Karch Celeste M.,Cooper Breanna,Skorupa Tara,Carrell David,Norton Joanne B.,Hsu Simon,Harari Oscar,Cai Yefei,Bertelsen Sarah,Goate Alison M.,Cruchaga Carlos

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Reference49 articles.

1. DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features;J. Exp. Med.,2003

2. The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2;Neurology,2005

3. An Italian family affected by Nasu–Hakola disease with a novel genetic mutation in the TREM2 gene;J. Neurol. Neurosurg. Psychiatry,2003

4. Nasu–Hakola disease with a splicing mutation of TREM2 in a Japanese family;Eur. J. Neurol.,2011

5. Mutations in TREM2 lead to pure early-onset dementia without bone cysts;Hum. Mutat.,2008

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