Two novel germline mutations (Y548X and K732X) of the MLH1 gene in Czech patients with hereditary nonpolyposis colorectal cancer
Human mutation.
2000 Aug ;
16 (2) :
181.
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid10923051
PubMed
10923051
DOI
10.1002/1098-1004(200008)16:2<181::aid-humu22>3.0.co;2-r
PII: 10.1002/1098-1004(200008)16:2<181::AID-HUMU22>3.0.CO;2-R
Knihovny.cz E-resources
- MeSH
- Adaptor Proteins, Signal Transducing MeSH
- Base Pair Mismatch MeSH
- Colorectal Neoplasms, Hereditary Nonpolyposis genetics MeSH
- Adult MeSH
- Nuclear Proteins MeSH
- Colorectal Neoplasms genetics MeSH
- Humans MeSH
- Lysine genetics MeSH
- Molecular Sequence Data MeSH
- MutL Protein Homolog 1 MeSH
- Neoplasm Proteins genetics MeSH
- Polymorphism, Genetic MeSH
- Carrier Proteins MeSH
- Tyrosine genetics MeSH
- Germ-Line Mutation genetics MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Adaptor Proteins, Signal Transducing MeSH
- Nuclear Proteins MeSH
- Lysine MeSH
- MLH1 protein, human MeSH Browser
- MutL Protein Homolog 1 MeSH
- Neoplasm Proteins MeSH
- Carrier Proteins MeSH
- Tyrosine MeSH
References provided by Crossref.org
Synchronous gastric and sebaceous cancers, a rare manifestation of MLH1-related Muir-Torre syndrome
International journal of clinical and experimental pathology.
2014 ;
7 (8) :
5196-202.
[epub] 20140715
