Cargando…
Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition
PURPOSE: Some 10% of familial adenomatous polyposis (FAP) and 80% of attenuated polyposis (AFAP) cases remain molecularly unexplained. We scrutinized such cases by exome-wide and targeted methods to search for novel susceptibility genes. METHODS: Exome sequencing was conducted on 40 unexplained (mai...
Autores principales: | Olkinuora, Alisa, Nieminen, Taina T., Mårtensson, Emma, Rohlin, Anna, Ristimäki, Ari, Koskenvuo, Laura, Lepistö, Anna, Gebre-Medhin, Samuel, Nordling, Margareta, Peltomäki, Päivi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752675/ https://www.ncbi.nlm.nih.gov/pubmed/30573798 http://dx.doi.org/10.1038/s41436-018-0405-x |
Ejemplares similares
-
Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents
por: Olkinuora, Alisa Petriina, et al.
Publicado: (2022) -
Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis
por: Nieminen, Taina T., et al.
Publicado: (2016) -
Molecular Basis of Mismatch Repair Protein Deficiency in Tumors from Lynch Suspected Cases with Negative Germline Test Results
por: Olkinuora, Alisa, et al.
Publicado: (2020) -
Testing for Lynch Syndrome in Endometrial Carcinoma: From Universal to Age-Selective MLH1 Methylation Analysis
por: Pasanen, Annukka, et al.
Publicado: (2022) -
Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations
por: Porkka, Noora, et al.
Publicado: (2017)