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Glomerular Expression of Type IV Collagen Chains in Normal and X-Linked Alport Syndrome Kidneys

Alport syndrome is an inherited nephropathy characterized by alterations of the glomerular basement membrane because of mutations in type IV collagen genes. COL4A5 mutations, causing X-linked Alport syndrome, frequently result in the loss of the α5 chains of type IV collagen in basement membranes. T...

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Detalhes bibliográficos
Main Authors: Heidet, Laurence, Cai, Yi, Guicharnaud, Liliane, Antignac, Corinne, Gubler, Marie-Claire
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2000
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1850092/
https://ncbi.nlm.nih.gov/pubmed/10854213
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