Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Detection of a heterozygous germline APC mutation in a three-generation family with familial adenomatous polyposis using targeted massive parallel sequencing in Vietnam
por: Giang, Hoa, et al.
Publicado: (2018) -
Diagnostic Value of hTERT mRNA and in Combination With AFP, AFP-L3%, Des-γ-carboxyprothrombin for Screening of Hepatocellular Carcinoma in Liver Cirrhosis Patients HBV or HCV-Related
por: Nguyen, Hoang Bac, et al.
Publicado: (2022) -
Mutations in the HBV PreS/S gene related to hepatocellular carcinoma in Vietnamese chronic HBV-infected patients
por: Thi Cam Huong, Nguyen, et al.
Publicado: (2022) -
APC gene mutations and colorectal adenomatosis in familial adenomatous polyposis
por: Ficari, F, et al.
Publicado: (2000) -
Attenuated familial adenomatous polyposis with desmoids caused by an APC mutation
por: Ikenoue, Tsuneo, et al.
Publicado: (2015)