Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations

BACKGROUND: Lynch syndrome, the most frequent hereditary colorectal cancer syndrome, is caused by defects in mismatch repair genes. Genetic testing is important in order to identify mutation carriers who can benefit from intensive surveillance programs. One of the challenges with genetic testing is...

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Detalles Bibliográficos
Autores principales: Sjursen, Wenche, McPhillips, Mary, Scott, Rodney J., Talseth‐Palmer, Bente A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799874/
https://www.ncbi.nlm.nih.gov/pubmed/27064304
http://dx.doi.org/10.1002/mgg3.198

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799874/
https://www.ncbi.nlm.nih.gov/pubmed/27064304
http://dx.doi.org/10.1002/mgg3.198

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