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Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disease characterized by gastrointestinal hamartomatous polyps and mucocutaneous melanin spots. Germline mutation of the serine/threonine kinase 11 (STK11) gene are responsible for PJS. In this study, we investigated the...
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| 發表在: | BMC Gastroenterol |
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| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4659168/ https://ncbi.nlm.nih.gov/pubmed/26607058 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12876-015-0397-9 |
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