An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2006.00704.x/fullpdf
Reference17 articles.
1. Relative frequency and morphology of cancers in STK11 mutation carriers;Lim;Gastroenterology,2004
2. Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients;Scott;Clin Genet,2002
3. Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families;Westerman;Hum Mutat,1999
4. Genetic heterogeneity in Peutz-Jeghers syndrome;Boardman;Hum Mutat,2000
5. Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma;Olschwang;J Med Genet,2001
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