A novel mutation in <it>STK11 </it>gene is associated with Peutz-Jeghers Syndrome in Indian patients
<p>Abstract</p> <p>Background</p> <p>Peutz-Jeghers syndrome (PJS) is a rare multi-organ cancer syndrome and understanding its genetic basis may help comprehend the molecular mechanism of familial cancer. A number of germ line mutations in the <it>STK11 </it>...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2006-09-01
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| Series: | BMC Medical Genetics |
| Online Access: | http://www.biomedcentral.com/1471-2350/7/73 |