Germline mismatch repair gene variants analyzed by universal sequencing in Japanese cancer patients

BACKGROUND: Lynch syndrome (LS) is the commonest inherited cancer syndrome caused by pathogenic variants of germline DNA mismatch repair (g.MMR) genes. Genome‐wide sequencing is now increasingly applied for tumor characterization, but not for g.MMR. The aim of this study was to evaluate the incidenc...

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Detalhes bibliográficos
Publicado no:Cancer Med
Main Authors: Kiyozumi, Yoshimi, Matsubayashi, Hiroyuki, Horiuchi, Yasue, Higashigawa, Satomi, Oishi, Takuma, Abe, Masato, Ohnami, Sumiko, Urakami, Kenichi, Nagashima, Takeshi, Kusuhara, Masatoshi, Miyake, Hidehiko, Yamaguchi, Ken
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
Assuntos:
Clinical Cancer Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6745857/
https://ncbi.nlm.nih.gov/pubmed/31386297
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cam4.2432
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