The study of Lynch syndrome in a special population reveals a strong founder effect and an unusual mutational mechanism in familial adenomatous polyposis

Detalles Bibliográficos
Autores principales: Siraj, Abdul K, Masoodi, Tariq, Bu, Rong, Parvathareddy, Sandeep Kumar, Siraj, Sarah, Alassiri, Ali, Al-Dayel, Fouad, Alkuraya, Fowzan S, Al-Kuraya, Khawla S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
PostScript
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569390/
https://www.ncbi.nlm.nih.gov/pubmed/31924657
http://dx.doi.org/10.1136/gutjnl-2019-320511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569390/
https://www.ncbi.nlm.nih.gov/pubmed/31924657
http://dx.doi.org/10.1136/gutjnl-2019-320511

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