Analysis of Disease Progression-Associated Gene Expression Profile in Fibrillin-1 Mutant Mice: New Insight into Molecular Pathogenesis of Marfan Syndrome

Marfan syndrome (MFS) is a dominantly inherited connective tissue disorder caused by mutations in the gene encoding fibrillin-1 (FBN1) and is characterized by aortic dilatation and dissection, which is the primary cause of death in untreated MFS patients. However, disease progression-associated chan...

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Detalles Bibliográficos
Autores principales: Kim, Koung Li, Choi, Chanmi, Suh, Wonhee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Applied Pharmacology 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975469/
https://www.ncbi.nlm.nih.gov/pubmed/24753820
http://dx.doi.org/10.4062/biomolther.2014.010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975469/
https://www.ncbi.nlm.nih.gov/pubmed/24753820
http://dx.doi.org/10.4062/biomolther.2014.010

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