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Absence of MutY homologue mutation in patients with multiple sporadic adenomatous polyps in Korea
AIM: Recently, germ-line mutation in the base excision repair gene MYH has been identified to cause a novel autosomal recessive form of familial adenomatous polyposis (FAP). Interestingly, a striking evidence for MYH mutations within different ethnic groups has been demonstrated. In this study, we s...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Co., Limited
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4066163/ https://ncbi.nlm.nih.gov/pubmed/16521226 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v12.i6.951 |
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