Germline variant in MSX1 identified in a Dutch family with clustering of Barrett’s esophagus and esophageal adenocarcinoma

The vast majority of esophageal adenocarcinoma cases are sporadic and caused by somatic mutations. However, over the last decades several families have been identified with clustering of Barrett’s esophagus and esophageal adenocarcinoma. This observation suggests that one or more hereditary factors...

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Detalles Bibliográficos
Autores principales: van Nistelrooij, A. M. J., van Marion, R., van Ijcken, W. F. J., de Klein, A., Wagner, A., Biermann, K., Spaander, M. C. W., van Lanschot, J. J. B., Dinjens, W. N. M., Wijnhoven, B. P. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999157/
https://www.ncbi.nlm.nih.gov/pubmed/29134539
http://dx.doi.org/10.1007/s10689-017-0054-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999157/
https://www.ncbi.nlm.nih.gov/pubmed/29134539
http://dx.doi.org/10.1007/s10689-017-0054-2

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