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Autor:
S B, Lee, S H, Kim, D W, Bell, D C, Wahrer, T A, Schiripo, M M, Jorczak, D C, Sgroi, J E, Garber, F P, Li, K E, Nichols, J M, Varley, A K, Godwin, K M, Shannon, E, Harlow, D A, Haber
Publikováno v:
Cancer research. 61(22)
Li Fraumeni Syndrome (LFS) is a multicancer phenotype, most commonly associated with germ-line mutations in TP53. In a kindred with LFS without an inherited TP53 mutation, we have previously reported a truncating mutation (1100delC) in CHK2, encoding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ceac849ec1041031c769751b3d31c178
https://pubmed.ncbi.nlm.nih.gov/11719428
https://pubmed.ncbi.nlm.nih.gov/11719428
