1.
Br J Cancer
; 92(6): 1126-9, 2005 Mar 28.
Artículo
en Inglés
| MEDLINE
| ID: mdl-15756273
RESUMEN
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.