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

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 caus...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awduron:	Hearle, N, Tomlinson, I, Lim, W, Murday, V, Swarbrick, E, Lim, G, Phillips, R, Lee, P, O'Donohue, J, Trembath, R, Morrison, P, Norman, A, Taylor, R, Hodgson, S, Lucassen, A, Houlston, R
Fformat:	Journal article
Iaith:	English
Cyhoeddwyd:	BioMed Central 2005

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