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Mutation analysis of related genes in hamartoma polyp tissue of Peutz-Jeghers syndrome
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare disease with clinical manifestations of pigmented spots on the lips, mucous membranes and extremities, scattered gastrointestinal polyps, and susceptibility to tumors. The clinical heterogeneity of PJS is obvious, and the relationship between clinic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201153/ https://www.ncbi.nlm.nih.gov/pubmed/32390703 http://dx.doi.org/10.3748/wjg.v26.i16.1926 |