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An APC Mutation in a Large Chinese Kindred With Familial Adenomatous Polyposis Was Identified Using Both Next Generation Sequencing and Simple STR Marker Haplotypes
BACKGROUND: Familial adenomatous polyposis (FAP) is an autosomal dominant disorder characterized primarily by the development of numerous adenomatous polyps in the colon and a high risk for colorectal cancer. FAP is caused by germline mutations of the adenomatous polyposis coli (APC) gene. The proba...
Autores principales: | Zhan, Qitao, Wang, Liya, Xu, Xiangrong, Sun, Yan, Li, Lejun, Qi, Xuchen, Chen, Feng, Wei, Xiaoming, Raff, Michael L., Yu, Ping, Jin, Fan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064715/ https://www.ncbi.nlm.nih.gov/pubmed/32194643 http://dx.doi.org/10.3389/fgene.2020.00191 |
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