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Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation
Alport syndrome (AS) is an inherited disorder characterized by glomerular basement membrane (GBM) abnormality and development of chronic kidney disease at an early age. The cause of AS is a genetic mutation in type IV collagen, and more than 80% of patients have X-linked AS (XLAS) with mutation in C...
Gorde:
| Argitaratua izan da: | Biochem Biophys Rep |
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| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Elsevier
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6295608/ https://ncbi.nlm.nih.gov/pubmed/30582011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbrep.2018.12.003 |
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