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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Kim, Hansoo, Kim, Hyo-Jong, Chi, Sung-Gil, Lee, Sang-Kil, Joo, Gwang-Ro, Dong, Seok-Ho, Kim, Byung-Ho, Chang, Young-Woon, Lee, Jung-Il, Chang, Rin
Format: Artigo
Idioma:Inglês
Publicat: Baishideng Publishing Group Co., Limited 2006
Matèries:
Rapid Communication
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars