APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.
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| Description | scientific article |
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author: Marília Cravo Pedro Lage Célia Baltazar Paula Chaves Cristina Albuquerque |
| Publication date | September 1, 2009 |
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| Missing/wrong data? | Edit Wikidata item |