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Gastroenterology
Volume 138, Issue 7
, Pages 2558-2560
, June 2010
Alu-Mediated Genomic Deletion of the Serine/Threonine Protein Kinase 11 (STK11) Gene in Peutz–Jeghers Syndrome
References
- Relative frequency and morphology of cancers in STK11 mutation carriers. Gastroenterology. 2004;126:1788–1794
- Cancer risks in LKB1 germline mutation carriers. Gut. 2006;55:984–990
- LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome. J Med Genet. 2006;43:e18
- High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. Hum Mutat. 2005;26:513–519
- Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. J Med Genet. 2006;43:e15
- . Alu sequences. FEBS Lett. 1997;417:1–5
Conflicts of interest The authors disclose no conflicts.
PII: S0016-5085(10)00546-9
doi: 10.1053/j.gastro.2010.03.061
© 2010 AGA Institute. Published by Elsevier Inc. All rights reserved.
« Previous
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Gastroenterology
Volume 138, Issue 7
, Pages 2558-2560
, June 2010

