Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families

  • Kanter-Smoler G
  • Fritzell K
  • Rohlin A
  • et al.
N/ACitations
Citations of this article
13Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

The dominantly inherited condition familial adenomatous polyposis (FAP) is caused by germline mutations in the APC gene. Finding the causative mutations has great implications for the families. Correlating the genotypes to the phenotypes could help to improve the diagnosis and follow-up of patients.

Cite

CITATION STYLE

APA

Kanter-Smoler, G., Fritzell, K., Rohlin, A., Engwall, Y., Hallberg, B., Bergman, A., … Nordling, M. (2008). Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families. BMC Medicine, 6(1). https://doi.org/10.1186/1741-7015-6-10

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free