Wikidata

(Q54397907)

English

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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title
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 (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19793053
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19793053%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 February 2020
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patient
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