Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors

Autor: Rahner, N., Brockschmidt, F.F., Steinke, V., Kahl, P., Becker, T., Vasen, H.F., Wijnen, J.T., Tops, C.J., Holinski-Feder, E., Ligtenberg, M.J.L., Spruijt, L., Gorgens, H., Stemmler, S., Kloor, M., Dietmaier, W., Schumacher, J., Nothen, Markus, Propping, P., Hoogerbrugge, N.

Publikováno v: Familial Cancer, 11, 1, pp. 19-26
Familial Cancer, 11, 19-26
Familial Cancer, 11(1), 19-26
Familial Cancer, 11(1), 19-26. Springer, Cham

Item does not contain fulltext Lynch syndrome (Hereditary non-polyposis colorectal cancer/HNPCC) is a cancer susceptibility syndrome which is caused by germline mutations in DNA mismatch repair (MMR) genes, in particular MLH1 and MSH2. A pathogenic g

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36511faad563d6a4ee054c32b06da56a
https://hdl.handle.net/2066/108765