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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The strongest association is with c.1552A>T mutation confirming that Lgi2 is the causative gene in the region.
创建时间：
2011-07-28
