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A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome
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Footnotes
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This work was supported by the Deutsche Krebshilfe (Grant 70–3027 Ma 1) and the Deutsche Forschungsgemeinschaft (Grant KR 1620/3−1 and−2).
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Conflict of interest: none declared.