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Advance in research on the correlation between genotypes of susceptible mutations and clinical phenotype of familial adenomatous polyposis / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 919-923, 2017.
Article in Chinese | WPRIM | ID: wpr-344145
ABSTRACT
Familial adenomatous polyposis (FAP) is one of the most common hereditary colorectal cancers. Its intestinal and extra-intestinal manifestations are correlated with mutation sties of the APC gene. Potential gene modulation sites in patients who have typical clinical manifestations but with unidentified APC mutations are also discussed, which included MUTYH gene, AXIN gene and certain epigenetic changes. With the generalization of Precision Medicine, to offer individualized treatment and surveillance strategy based on the genotype-phenotype correlation will be of great value for FAP patients. This review focuses on the research advance in genotype - phenotype correlation studies of FAP patients.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Genes, APC / Adenomatous Polyposis Coli / Genetic Predisposition to Disease / DNA Glycosylases / Beta Catenin / Genetic Association Studies / Axin Protein / Genetics / Mutation Limits: Humans Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2017 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Genes, APC / Adenomatous Polyposis Coli / Genetic Predisposition to Disease / DNA Glycosylases / Beta Catenin / Genetic Association Studies / Axin Protein / Genetics / Mutation Limits: Humans Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2017 Type: Article