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Additional file 1: of The Trem2 R47H variant confers loss-of-function-like phenotypes in Alzheimer’s disease

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Figshare2018-06-02 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Additional_file_1_of_The_Trem2_R47H_variant_confers_loss-of-function-like_phenotypes_in_Alzheimer_s_disease/6407066
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Table S1. Variant calling for APPPS1–21;Trem2 +/R47H mice for the CRISPR predicted off target gene Rab11fip3, Trem2, and Trem-like genes Treml1, Treml2, and Treml6. “0/1” indicates a heterozygous variant and “./.” indicates no variants detected. Variants detected in Trem2 R47H lines but not APPPS1–21; Trem2+/+ or Trem2+/+ mice were considered to be true. (XLSX 14 kb)
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2018-06-02
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