Nonetheless, in Neupane et al., exploratory analysis of exonic variants of our candidate genes identified three nominally significant loci (single variants in C2CD3 and NALCN , and a region with 39 rare variants in CTNNA2 with a p‐value of 0.05, which the authors did not discuss).
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Reply to Neupane et al.: Replication study of AD-associated rare variants.
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