Sequence changes in predicted promoter elements of <it>STK11/LKB1 </it>are unlikely to contribute to Peutz-Jeghers syndrome

<p>Abstract</p> <p>Background</p> <p>Germline mutations or large-scale deletions in the coding region and splice sites of <it>STK11/LKB1 </it>do not account for all cases of Peutz-Jeghers syndrome (PJS). It is conceivable that, on the basis of data from other diseases, inherited variation in promote...

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Hlavní autoři:	Morrison Patrick J, Trembath Richard C, O'Donohue John, Lee Peter, Phillips Robin, Lim Guan, Swarbrick Edwin, Murday Victoria, Lim Wendy, Tomlinson Ian, Hearle Nicholas CM, Norman Andrew, Taylor Rohan, Hodgson Shirley, Lucassen Anneke, Houlston Richard S
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2005-03-01
Edice:	BMC Genomics
On-line přístup:	http://www.biomedcentral.com/1471-2164/6/38
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