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First Polish Cowden syndrome patient with confirmed PTEN gene mutation
Cowden syndrome is a rare hereditary disease. Incidence of the disease is conditioned by occurrence of mutations in the PTEN gene. The disease has a frequency of 1/120,000 newborn and it predisposes to the occurrence of hamartoma polyps in the gastrointestinal tract, skin tumours, as well as tumours...
में बचाया:
| मुख्य लेखकों: | , , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Termedia Publishing House
2010
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3278958/ https://ncbi.nlm.nih.gov/pubmed/22371735 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5114/aoms.2010.13522 |
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