Sporadic Case of Heterozygous X-linked Alport Syndrome
Background: Alport syndrome is a genetically and phenotypically heterogeneous disorder that can be transmitted in an X-linked, autosomal recessive, or autosomal dominant fashion and can affect glomerular, cochlear, and ocular basement membranes. The disorder results from mutations in the collagen IV...
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Karger Publishers
2023-05-01
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| Colección: | Glomerular Diseases |
| Acceso en línea: | https://beta.karger.com/Article/FullText/530994 |
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