Non-collagen genes role in digenic Alport syndrome

BACKGROUND: Alport syndrome is a clinically heterogeneous nephropathy characterized by severe symptomatology at kidney level due to ultrastructural lesions of the glomerular basement membrane (GBM) as consequence of mutations in COL4 genes. The disease has been linked to COL4A3/COL4A4/COL4A5 mutatio...

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Detalles Bibliográficos
Autores principales: Daga, S., Fallerini, C., Furini, S., Pecoraro, C., Scolari, F., Ariani, F., Bruttini, M., Mencarelli, M. A., Mari, F., Renieri, A., Pinto, A. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391820/
https://www.ncbi.nlm.nih.gov/pubmed/30808327
http://dx.doi.org/10.1186/s12882-019-1258-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391820/
https://www.ncbi.nlm.nih.gov/pubmed/30808327
http://dx.doi.org/10.1186/s12882-019-1258-5

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