Chapter 15 Brain Tumors and the Lynch Syndrome

By: Contributor(s): Material type: ArticleArticleLanguage: English Publication details: InTechOpen 2011ISBN:
  • 21293
Subject(s): Online resources: Summary: 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).
Item type:
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
No physical items for this record

Open Access star Unrestricted online access

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).

Creative Commons https://creativecommons.org/licenses/by-nc-sa/3.0/ cc https://creativecommons.org/licenses/by-nc-sa/3.0/

English

There are no comments on this title.

to post a comment.
Share