The Mutation Spectrum and Two Novel Point Mutations in the APC Gene in Vietnamese Patients with Familial Adenomatous Polyposis

BACKGROUND: Familial adenomatous polyposis (FAP) is a hereditary disorder primarily caused by germline mutations in the APC gene. The most common type of mutation in the APC gene is point mutation, while deletion mutation is much less frequent. The current study was conducted to investigate the muta...

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Detalles Bibliográficos
Autores principales: Nguyen, Bac Hoang, Nguyen, Suong Thi Bang, Nguyen, Huy Huu, Nguyen, Tin Trung, Le, Khoi Minh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: West Asia Organization for Cancer Prevention 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587892/
https://www.ncbi.nlm.nih.gov/pubmed/35633533
http://dx.doi.org/10.31557/APJCP.2022.23.5.1517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9587892/
https://www.ncbi.nlm.nih.gov/pubmed/35633533
http://dx.doi.org/10.31557/APJCP.2022.23.5.1517

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