Functional characterization ofMLH1missense variants identified in lynch syndrome patients-Reference-Cited by-同舟云学术

Functional characterization ofMLH1missense variants identified in lynch syndrome patients

Published:2012-07-23 Issue:12 Volume:33 Page:1647-1655
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Andersen Sofie Dabros,Liberti Sascha Emilie,Lützen Anne,Drost Mark,Bernstein Inge,Nilbert Mef,Dominguez Mev,Nyström Minna,Hansen Thomas Van Overeem,Christoffersen Janus Wiese,Jäger Anne Charlotte,de Wind Niels,Nielsen Finn Cilius,Tørring Pernille M.,Rasmussen Lene Juel

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22153/fullpdf

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4. Characterization of the nuclear import of human MutL alpha;Brieger;Mol Carcinogen,2005

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