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Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane.

Alport-type familial nephritis (FN), a genetic disorder, results in progressive renal insufficiency and sensorineural hearing loss. Immunochemical and biochemical analyses of the non-collagenous (NC1) domain of type IV collagen isolated from the glomerular basement membranes (GBM) of three males wit...

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Bibliografski detalji
Glavni autori: Kleppel, M M, Kashtan, C E, Butkowski, R J, Fish, A J, Michael, A F
Format: Artigo
Jezik:Inglês
Izdano: 1987
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC442227/
https://ncbi.nlm.nih.gov/pubmed/3298322
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