TY  - CHAP
AU  - Peltomäki, Päivi
AU  - Gylling, Annette
AB  - Lynch syndrome (LS) (MIM No. 120435-6), previously known as hereditary nonpolyposis colorectal cancer (HNPCC) (Boland, 2005), is an autosomal dominant disorder caused by    germline mutation in one of the DNA mismatch repair (MMR) genes. LS is among the most    prevalent cancer syndromes in man and is estimated to account for 1-6% of all colorectal    cancers (Lynch & de la Chapelle, 2003).
DO  - 10.5772/21293
ID  - OAPEN ID: 612584
ID  - OAPEN ID: OCN: 1030821093
ID  - OAPEN ID: http://library.oapen.org/handle/20.500.12657/32348
KW  - brain tumors
KW  - lynch syndrome
KW  - brain tumors
KW  - lynch syndrome
KW  - Colorectal cancer
KW  - DNA methylation
KW  - DNA mismatch repair
KW  - Gene
KW  - Glioblastoma
KW  - Glioma
KW  - Hereditary nonpolyposis colorectal cancer
KW  - Mutation
KW  - Neoplasm
L1  - https://library.oapen.org/bitstream/20.500.12657/32348/1/612584.pdf
L1  - https://library.oapen.org/bitstream/20.500.12657/32348/1/612584.pdf
L1  - https://library.oapen.org/bitstream/20.500.12657/32348/1/612584.pdf
LA  - English
LK  - https://directory.doabooks.org/handle/20.500.12854/37172
PB  - InTechOpen
PY  - 2011
TI  - Chapter 15 Brain Tumors and the Lynch Syndromenull
ER  - 
