The Peutz-Jeghers syndrome (PJS) is a rare hereditary disorder in which gastrointestinal hamartomatous polyposis, mucocutaneous pigmentation, and a predisposition for developing cancer are transmitted in an autosomal dominant fashion. The recently identified LKB1/STK11 gene located at chromosome 19p
β¦ LIBER β¦
Mutations analysis ofSTK11gene in Chinese families with Peutz-Jeghers syndrome
β Scribed by Lianchun Kang; Xirong Zhao; Yongshuang Zhou; Yixing Jia; Suhai Kang; Zhu Chen; Min Zhao; Jiantao Cui; Wenmei Li; Anle Sun; Youyong Lu
- Publisher
- Springer
- Year
- 2003
- Tongue
- English
- Weight
- 519 KB
- Volume
- 48
- Category
- Article
- ISSN
- 1001-6538
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