Sequence changes in predicted promoter elements of <it>STK11/LKB1 </it>are unlikely to contribute to Peutz-Jeghers syndrome
<p>Abstract</p> <p>Background</p> <p>Germline mutations or large-scale deletions in the coding region and splice sites of <it>STK11/LKB1 </it>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 promote...
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| Principais autores: | , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BMC
2005-03-01
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| Series: | BMC Genomics |
| Acceso en liña: | http://www.biomedcentral.com/1471-2164/6/38 |
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