A novel POLD1 pathogenic variant identified in two families with a cancer spectrum mimicking Lynch syndrome.
Legrand C, Lebrun M, Naïbo P, Peysselon M, Prieur F, Kientz C, Desseigne F, Handallou S, Rey JM, Nambot S, Goussot V, Hamzaoui N, Wang Q.
Legrand C, et al. Among authors: kientz c.
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Eur J Med Genet. 2022.
PMID: 34954152