Síndrome de Lynch: Caracterización genético clínica. Caso clínico
Hereditary non-polyposis colorectal cancer (HNPCC) or Lynch Syndrome is an autosomic dominant syndrome involving 596-1096 of colorectal cancer patients. Mutations in MLH1 and MSH2 genes account for most cases. These two genes particípate in the DNA mismatch repair pathway. Therefore mutation carrier...
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| Main Authors: | , , , , , , |
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| Language: | Spanish / Castilian |
| Published: |
Sociedad Médica de Santiago
2008
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| Subjects: | |
| Online Access: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872008000600011 |
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