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A novel POLD1 pathogenic variant identified in two families with a cancer spectrum mimicking Lynch syndrome

Document Type

Article

Author

Legrand, C.; Peysselon, M.; Lebrun, M.; Prieur, F.; Kientz, C.; Naïbo, P.; Wang, Q.; Desseigne, F.; Handallou, S.; Rey, J.-M.; Nambot, S.; Goussot, V.; Hamzaoui, N.

Source

In: European Journal of Medical Genetics. (European Journal of Medical Genetics, February 2022, 65(2))

Subject

Language

English

ISSN

18780849
17697212

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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