A Marfan syndrome gene expression phenotype in cultured skin fibroblasts

BACKGROUND: Marfan syndrome (MFS) is a heritable connective tissue disorder caused by mutations in the fibrillin-1 gene. This syndrome constitutes a significant identifiable subtype of aortic aneurysmal disease, accounting for over 5% of ascending and thoracic aortic aneurysms. RESULTS: We used spot...

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Detalles Bibliográficos
Autores principales: Yao, Zizhen, Jaeger, Jochen C, Ruzzo, Walter L, Morale, Cecile Z, Emond, Mary, Francke, Uta, Milewicz, Dianna M, Schwartz, Stephen M, Mulvihill, Eileen R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174953/
https://www.ncbi.nlm.nih.gov/pubmed/17850668
http://dx.doi.org/10.1186/1471-2164-8-319

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174953/
https://www.ncbi.nlm.nih.gov/pubmed/17850668
http://dx.doi.org/10.1186/1471-2164-8-319

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