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

BACKGROUND: Germline mutations or large-scale deletions in the coding region and splice sites of STK11/LKB1 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 promoter elements of STK11/LKB1 may cause...

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Detalles Bibliográficos
Autores principales: Hearle, Nicholas CM, Tomlinson, Ian, Lim, Wendy, Murday, Victoria, Swarbrick, Edwin, Lim, Guan, Phillips, Robin, Lee, Peter, O'Donohue, John, Trembath, Richard C, Morrison, Patrick J, Norman, Andrew, Taylor, Rohan, Hodgson, Shirley, Lucassen, Anneke, Houlston, Richard S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1084245/
https://www.ncbi.nlm.nih.gov/pubmed/15774015
http://dx.doi.org/10.1186/1471-2164-6-38

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