Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome

Peutz-Jeghers syndrome (PJS), a rare autosomal dominant inherited disorder, is characterized by hamartomatous gastrointestinal polyps and mucocutaneous pigmentation. Patients with this syndrome have a predisposition to a variety of cancers in multiple organs. Mutations in the serine/threonine kinase...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Ausavarat, Surasawadee, Leoyklang, Petcharat, Vejchapipat, Paisarn, Chongsrisawat, Voranush, Suphapeetiporn, Kanya, Shotelersuk, Vorasuk
Formato: Artigo
Lenguaje:Inglês
Publicado: The WJG Press and Baishideng 2009
Materias:
Case Report
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2776867/
https://ncbi.nlm.nih.gov/pubmed/19908348
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.15.5364
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares