PubMed:15289847 / 253-383 JSONTXT

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    PubMed_ArguminSci

    {"project":"PubMed_ArguminSci","denotations":[{"id":"T2","span":{"begin":0,"end":130},"obj":"DRI_Background"}],"text":"HNPCC is caused by a constitutional defect in a mismatch repair (MMR) gene, most commonly affecting the genes MLH1, MSH2 and MSH6."}