A modifying locus for familial adenomatous polyposis may be present on chromosome 1p35-p36.
Mutations of the APC gene cause familial adenomatous polyposis (FAP) in humans and multiple intestinal neoplasia (Min) in laboratory mouse strains. A dominant modifying gene (Mom1), which partially suppresses the min phenotype, has been mapped to mouse chromosome 4. This region is syntenic with huma...
Main Authors: | , , , , , , |
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Format: | Journal article |
Language: | English |
Published: |
1996
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