Case Report: The Role of Molecular Analysis of the MUTYH Gene in Asymptomatic Individuals

MUTYH-associated polyposis (MAP) is a rare hereditary condition caused by the biallelic mutation in the MUTYH gene encoding MUTYH glycosylase. This enzyme is a key member of the base excision repair (BER) pathway responsible for the repair of DNA lesions formed by reactive oxygen species (ROS). We r...

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Detalles Bibliográficos
Autores principales: Fabišíková, Katarína, Hamidová, Olívia, Behulová, Regína Lohajová, Závodná, Katarína, Priščáková, Petra, Repiská, Vanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770176/
https://www.ncbi.nlm.nih.gov/pubmed/33384714
http://dx.doi.org/10.3389/fgene.2020.590486

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770176/
https://www.ncbi.nlm.nih.gov/pubmed/33384714
http://dx.doi.org/10.3389/fgene.2020.590486

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