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BioMed Central, Hereditary Cancer in Clinical Practice, 1(8), 2010

DOI: 10.1186/1897-4287-8-7

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A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome

Journal article published in 2010 by Els van Riel, Margreet Gem Ausems, Frans Bl Hogervorst, Irma Kluijt, Marielle E. van Gijn, Jeanne van Echtelt, Karen Scheidel-Jacobse, Eric Fam Hennekam, Rein P. Stulp, Yvonne J. Vos, G. Johan A. Offerhaus, G. Johan A. Offerhaus, Fred H. Menko, Johan Jp Gille ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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