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Br J Cancer ; 92(6): 1126-9, 2005 Mar 28.
Article in English | MEDLINE | ID: mdl-15756273

ABSTRACT

Mutations in LKB1 lead to Peutz-Jeghers syndrome (PJS). However, only a subset of PJS patients harbours LKB1 mutations. We performed a mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in 28 LKB1-negative PJS patients. No disease-causing mutations were detected in the studied genes in PJS patients from different European populations.


Subject(s)
Adaptor Proteins, Signal Transducing/genetics , Adaptor Proteins, Vesicular Transport/genetics , Mutation , Nuclear Proteins/genetics , Peutz-Jeghers Syndrome/genetics , Transcription Factors/genetics , DNA Helicases , Humans , Introns , Polymorphism, Genetic
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