Omslagsbild

Chapter 15 Brain Tumors and the Lynch Syndrome

Visa andra versioner (1)

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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudskapare: Peltomäki, Päivi (auth)
Övriga skapare: Gylling, Annette (auth)
Materialtyp: Elektronisk Bokavsnitt
Språk:engelska
Publicerad: InTechOpen 2011
Ämnen:
Science: general issues
brain tumors
lynch syndrome
Colorectal cancer
DNA methylation
DNA mismatch repair
Gene
Glioblastoma
Glioma
Hereditary nonpolyposis colorectal cancer
Mutation
Neoplasm
Länkar:OAPEN Library: download the publication
OAPEN Library: description of the publication
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!
Visa alla versioner (2)

Liknande verk