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...

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التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	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
التنسيق:	Journal article
اللغة:	English
منشور في:	BioMed Central 2005

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

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