Is HSPG2 a modifier gene for Marfan syndrome?

Marfan syndrome (MFS) is a connective tissue disease caused by variants in the FBN1 gene. Nevertheless, other genes influence the manifestations of the disease, characterized by high clinical variability even within families. We mapped modifier loci for cardiovascular and skeletal manifestations in...

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Detalles Bibliográficos
Autores principales: Gerdes Gyuricza, Isabela, Barbosa de Souza, Rodrigo, Farinha-Arcieri, Luis Ernesto, Ribeiro Fernandes, Gustavo, Veiga Pereira, Lygia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608216/
https://www.ncbi.nlm.nih.gov/pubmed/32514132
http://dx.doi.org/10.1038/s41431-020-0666-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608216/
https://www.ncbi.nlm.nih.gov/pubmed/32514132
http://dx.doi.org/10.1038/s41431-020-0666-0

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