The 2014 International Workshop on Alport Syndrome

Alport syndrome, historically referred to as hereditary glomerulonephritis with sensorineural deafness and anterior lenticonus, is a genetic disease of collagen α3α4α5(IV) resulting in renal failure. The collagen α3α4α5(IV) heterotrimer forms a network that is a major component of the kidney glomeru...

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Detalles Bibliográficos
Autores principales: Miner, Jeffrey H, Baigent, Colin, Flinter, Frances, Gross, Oliver, Judge, Parminder, Kashtan, Clifford E, Lagas, Sharon, Savige, Judith, Blatt, Dave, Ding, Jie, Gale, Daniel P, Midgley, Julian P, Povey, Sue, Prunotto, Marco, Renault, Daniel, Skelding, Jules, Turner, A Neil, Gear, Susie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Meeting Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182137/
https://www.ncbi.nlm.nih.gov/pubmed/24988067
http://dx.doi.org/10.1038/ki.2014.229

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182137/
https://www.ncbi.nlm.nih.gov/pubmed/24988067
http://dx.doi.org/10.1038/ki.2014.229

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