TREM2 and neurodegenerative disease

New England Journal of Medicine

Volumn 369, Issue 16, 2013, Pages 1564-1570

  Reitz, Christiane ^a   Mayeux, Richard ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC MARKER; GENOTYPE; HUMAN; LETTER; MOLECULAR PATHOLOGY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TRIGGERING RECEPTOR EXPRESSED ON MYELOID CELLS 2 GENE; ANIMAL; GENETICS; MISSENSE MUTATION; MUTATION; NOTE; AUTOSOMAL RECESSIVE DISORDER; BRAIN DISEASE; DEGENERATIVE DISEASE; GENE EXPRESSION; GENE IDENTIFICATION; GENE LOCUS; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HIGH RISK POPULATION; LOSS OF FUNCTION MUTATION; MEMBRANOUS LIPODYSTROPHY; RISK ASSESSMENT; TREM2 GENE;

IMMUNOGLOBULIN RECEPTOR; MEMBRANE PROTEIN;

ALZHEIMER DISEASE; ANIMALS; HUMANS; MEMBRANE GLYCOPROTEINS; MUTATION; MUTATION, MISSENSE; RECEPTORS, IMMUNOLOGIC;

EID: 84885761556     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMc1306509     Document Type: Letter

References (3)

1. Guerreiro R, Wojtas A, Bras J, et al. TREM2 variants in Alzheimer's disease. N Engl J Med 2013;368:117-27.
2. Jonsson T, Stefansson H, Steinberg S, et al. Variant of TREM2 associated with the risk of Alzheimer's disease. N Engl J Med 2013;368:107-16.
3. Liu JZ, McRae AF, Nyholt DR, et al. A versatile gene-based test for genome-wide association studies. Am J Hum Genet 2010;87:139-45.