A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome

BACKGROUND: Peutz-Jeghers syndrome (PJS) is an unusual autosomal dominant disorder characterized by mucocutaneous pigmentation and multiple gastrointestinal hamartomatous polyps. Patients with PJS are at an increased risk of developing multi-organ cancer, most frequently those involving the gastroin...

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Detalles Bibliográficos
Autores principales: Yoo, Jong-Ha, Yoo, Jee-Hyoung, Choi, Yoon-Jung, Kang, Jung-Gu, Sun, Young-Kyu, Ki, Chang-Seok, Lee, Kyung-A, Choi, Jong-Rak
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2430547/
https://www.ncbi.nlm.nih.gov/pubmed/18495044
http://dx.doi.org/10.1186/1471-2350-9-44

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