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CGE.12062
CGE.12062
http://dx.doi.org/10.1111/CGE.12062
The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families.
P356
Q50894957-57E588FE-A29B-45CA-A659-4F1BC6908D7D
P356
CGE.12062
http://dx.doi.org/10.1111/CGE.12062