Cargando…
Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-to-CMMRD Phenotypic Continuum
Lynch syndrome (LS) is the most common hereditary colorectal cancer (CRC) syndrome, caused by heterozygous mutations in the mismatch repair (MMR) genes. Biallelic mutations in these genes lead however, to constitutive mismatch repair deficiency (CMMRD). In this study, we follow the diagnostic journe...
Autores principales: | Fernández-Rozadilla, Ceres, Alvarez-Barona, Miriam, Schamschula, Esther, Bodo, Sahra, Lopez-Novo, Anael, Dacal, Andres, Calviño-Costas, Consuelo, Lancho, Angel, Amigo, Jorge, Bello, Xabier, Cameselle-Teijeiro, Jose Manuel, Carracedo, Angel, Colas, Chrystelle, Muleris, Martine, Wimmer, Katharina, Ruiz-Ponte, Clara |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721314/ https://www.ncbi.nlm.nih.gov/pubmed/31366136 http://dx.doi.org/10.3390/cancers11081081 |
Ejemplares similares
-
Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019
por: Suerink, M., et al.
Publicado: (2020) -
HGG-40. NF1 mosaicism in a CMMRD-patient with a glioblastoma
por: Guerrini-Rousseau, Lea, et al.
Publicado: (2022) -
Liquid Biopsy Biomarkers for Immunotherapy in Non-Small Cell Lung Carcinoma: Lessons Learned and the Road Ahead
por: Hita-Millan, Jesus, et al.
Publicado: (2021) -
Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer
por: Fernández-Rozadilla, C., et al.
Publicado: (2021) -
Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula
por: Bycroft, Clare, et al.
Publicado: (2019)