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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Autor principal: Peltomäki, Päivi (auth)
Otros Autores: Gylling, Annette (auth)
Formato: Electrónico Capítulo de libro
Lenguaje:inglés
Publicado: InTechOpen 2011
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