@article{55c905e73b12432baf6b6603b9691436,
title = "A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic one",
keywords = "Functional analysis, Lynch syndrome, MSH2, MSH6, Variants of uncertain significance (VUS), NONPOLYPOSIS COLORECTAL-CANCER, DNA MISMATCH REPAIR, GERMLINE MUTATIONS, MISSENSE MUTATIONS, MUTS-ALPHA, HNPCC, PROTEIN, CELLS, GENE, 1184 Genetics, developmental biology, physiology",
author = "Jukka Kantelinen and Hansen, {Thomas V. O.} and Minttu Kansikas and Krogh, {Lotte Nylandsted} and Korhonen, {Mari K.} and Saara Ollila and Minna Nystrom and Anne-Marie Gerdes and Reetta Kariola",
year = "2011",
doi = "10.1007/s10689-011-9436-z",
language = "English",
volume = "2011",
pages = "515--520",
journal = "Familial Cancer",
issn = "1389-9600",
publisher = "Springer Science and Business Media B.V.",
number = "10",
}