Mutations in the humanLKB1/STK11gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference74 articles.
1. Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597 (insertion mark) 598insIVS4);Abed;Hum Mutat,2001
2. Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in Peutz-Jeghers syndrome;Alhopuro;Br J Cancer,2005
3. Genotype-phenotype correlations in Peutz-Jeghers syndrome;Amos;J Med Genet,2004
4. Somatic mutations in LKB1 are rare in sporadic colorectal and testicular tumors;Avizienyte;Cancer Res,1998
5. LKB1 somatic mutations in sporadic tumors;Avizienyte;Am J Pathol,1999
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