The 2014International 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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Bibliographic Details
Main Authors: Miner, J, Baigent, C, Flinter, F, Gross, O, Judge, P, Kashtan, C, Lagas, S, Savige, J, Blatt, D, Ding, J, Gale, D, Midgley, J, Povey, S, Prunotto, M, Renault, D, Skelding, J, Turner, A, Gear, S
Format: Journal article
Language:English
Published: 2014