Genome-wide methylation patterns in Marfan syndrome

BACKGROUND: Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in the Fibrillin-1 gene (FBN1). Here, we undertook the first epigenome-wide association study (EWAS) in patients with MFS aiming at identifying DNA methylation loci associated with MFS phenotypes that may shed ligh...

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Detalles Bibliográficos
Autores principales: van Andel, Mitzi M., Groenink, Maarten, van den Berg, Maarten P., Timmermans, Janneke, Scholte, Arthur J. H. A., Mulder, Barbara J. M., Zwinderman, Aeilko H., de Waard, Vivian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665617/
https://www.ncbi.nlm.nih.gov/pubmed/34895303
http://dx.doi.org/10.1186/s13148-021-01204-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665617/
https://www.ncbi.nlm.nih.gov/pubmed/34895303
http://dx.doi.org/10.1186/s13148-021-01204-4

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