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140 O - Molecular analysis of APC mutations in familial adenomatous polyposis

✍ Scribed by M. De Rosa; M.I. Scarano; A. Nappo; L. Panariello; N. Carlomagno; A. Renda; G.B. Rossi; F. Salvatore; P. Izzo

Book ID
116168412
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
208 KB
Volume
32
Category
Article
ISSN
0959-8049

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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

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## Communicated by Georgia Chenevix-Trench Familial adenomatous polyposis (FAP) is an autosomal dominantly inherited predisposition to colorectal cancer, which is caused by germline mutations in the adenomatous polyposis coli (APC) gene. The APC mutations have been investigated in 46 Czech unrelat