The American founder mutation for Lynch syndrome: Prevalence and cancer control implications
| Autor: | Riccardo Fodde, Henry T. Lynch, Gordon Gong, M. B. Clark, A. de la Chapelle, Heather Hampel, Gleb Haynatzki, Stephanie Coronel, Ross A. Okimoto, Abdon Trowonou, Anja Wagner |
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| Rok vydání: | 2005 |
| Předmět: |
Genetics
congenital hereditary and neonatal diseases and abnormalities Cancer Research nutritional and metabolic diseases Biology medicine.disease digestive system diseases Lynch syndrome law.invention Exon Oncology Cancer control law medicine Msh2 gene neoplasms Founder mutation Polymerase chain reaction |
| Zdroj: | Journal of Clinical Oncology. 23:9505-9505 |
| ISSN: | 1527-7755 0732-183X |
| Popis: | 9505 Background: We have recently reported a new founder mutation, namely, an exon 1–6 deletion in the MSH2 gene detectable by a recently designed single PCR reaction in 9 kindreds with Lynch Syndr... |
| Databáze: | OpenAIRE |
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