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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2014
Pynciau:
Meeting Report
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4182137/
https://ncbi.nlm.nih.gov/pubmed/24988067
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ki.2014.229
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