Chapter 15 Brain Tumors and the Lynch Syndrome
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 e...
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| Formaat: | Elektronisch Hoofdstuk |
| Taal: | Engels |
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InTechOpen
2011
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| Online toegang: | OAPEN Library: download the publication OAPEN Library: description of the publication |
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