Wordt geladen...
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...
Bewaard in:
| Hoofdauteurs: | , , , , , , , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Baishideng Publishing Group Co., Limited
2006
|
| Onderwerpen: | |
| Online toegang: | 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 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|