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Four highly-associated SNPs spread across the linked 1.7 Mb homozygosity region, together with the c.1552A>T mutation, were genotyped and tested for association from 28 BFJE cases and 112 healthy controls.

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Figshare2015-12-02 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_Four_highly_associated_SNPs_spread_across_the_linked_1_7_Mb_homozygosity_region_together_with_the_c_1552A_gt_T_mutation_were_genotyped_and_tested_for_association_from_28_BFJE_cases_and_112_healthy_controls_/421145
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The strongest association is with c.1552A>T mutation confirming that Lgi2 is the causative gene in the region.
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2015-12-02
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