A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer risk.
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HGG Adv. 2021 Dec 10;3(1):100078. doi: 10.1016/j.xhgg.2021.100078. eCollection 2022 Jan 13.
HGG Adv. 2021.
PMID: 35047863
Free PMC article.