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Genetics of Alzheimer's Disease
被引:61
|作者:
Ridge, Perry G.
[1
]
Ebbert, Mark T. W.
[1
,2
]
Kauwe, John S. K.
[1
]
机构:
[1] Brigham Young Univ, Dept Biol, Provo, UT 84602 USA
[2] ARUP Inst Clin & Expt Pathol, Salt Lake City, UT 84108 USA
关键词:
AMYLOID PRECURSOR PROTEIN;
MULTIFACTOR-DIMENSIONALITY REDUCTION;
GENOME-WIDE ASSOCIATION;
SINGLE NUCLEOTIDE POLYMORPHISMS;
PLASMA CLUSTERIN CONCENTRATION;
MITOCHONDRIAL-DNA HAPLOGROUPS;
CLATHRIN ASSEMBLY PROTEIN;
HIGH-ORDER INTERACTIONS;
COMPLEMENT RECEPTOR 1;
APOLIPOPROTEIN-E;
D O I:
10.1155/2013/254954
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Alzheimer's disease is the most common form of dementia and is the only top 10 cause of death in the United States that lacks disease-altering treatments. It is a complex disorder with environmental and genetic components. There are two major types of Alzheimer's disease, early onset and the more common late onset. The genetics of early-onset Alzheimer's disease are largely understood with variants in three different genes leading to disease. In contrast, while several common alleles associated with late-onset Alzheimer's disease, including APOE, have been identified using association studies, the genetics of late-onset Alzheimer's disease are not fully understood. Here we review the known genetics of early- and late-onset Alzheimer's disease.
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