Recurrent and founder mutations in the PMS2 gene

Germline mutations in PMS2 are associated with Lynch syndrome (LS), the most common known cause of hereditary colorectal cancer. Mutation detection in PMS2 has been difficult due to the presence of several pseudogenes, but a custom-designed long-range PCR strategy now allows adequate mutation detect...

Descrición completa

Gardado en:
Detalles Bibliográficos
Main Authors: Tomsic, Jerneja, Senter, Leigha, Liyanarachchi, Sandya, Clendenning, Mark, Vaughn, Cecily P., Jenkins, Mark A., Hopper, John L., Young, Joanne, Samowitz, Wade, de la Chapelle, Albert
Formato: Artigo
Idioma:Inglês
Publicado: 2012
Assuntos:
Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3445698/
https://ncbi.nlm.nih.gov/pubmed/22577899
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2012.01898.x
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares