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Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients

✍ Scribed by Markos Mihalatos; Angela Apessos; Hans Dauwerse; Voula Velissariou; Aristidis Psychias; Alexander Koliopanos; Konstantinos Petropoulos; John K Triantafillidis; Ioannis Danielidis; George Fountzilas; Niki J Agnantis; Georgios Nasioulas

Book ID
115010699
Publisher
BioMed Central
Year
2005
Tongue
English
Weight
347 KB
Volume
5
Category
Article
ISSN
1471-2407

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## Development of one hundred or more adenomas in the colon and rectum is diagnostic for the dominantly inherited, autosomal disease Familial Adenomatous Polyposis (FAP). It is possible to identify a mutation in the Adenomatous Polyposis Coli (APC) gene in approximately 80% of the patients, and alm