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Glomerular pathology in Alport syndrome: a molecular perspective
We have known for some time that mutations in the genes encoding 3 of the 6 type IV collagen chains are the underlying defect responsible for both X-linked (where the COL4A5 gene is involved) and autosomal (where either COL4A3 or COL4A4 genes are involved) Alport syndrome. The result of these mutati...
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2011
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| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3484979/ https://ncbi.nlm.nih.gov/pubmed/21455721 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-011-1868-z |
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