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A new family with a homozygous nonsense variant in NTHL1 further delineated the clinical phenotype of NTHL1-associated polyposis

Crossref DOI link: https://doi.org/10.1038/s41439-019-0077-3

Published Online: 2019-10-10

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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