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注意：仅列出部分参考文献，下载原文获取全部文献信息。A novel homozygous mutation in TREM2 found in a Chinese early-onset dementia family with mild bone involvement
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Coding variants in TREM2 increase risk for Alzheimer's disease
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Homozygous TREM2 mutation in a family with atypical frontotemporal dementia
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Mutations in TREM2 Lead to Pure Early-Onset Dementia Without Bone Cysts
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Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype
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