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Genotype‐phenotype correlation and prognostic impact in Chinese patients with Alport Syndrome
BACKGROUND: Alport Syndrome (AS) is a progressive hereditary glomerular disease. It is often accompanied by sensorineural hearing loss and ocular abnormalities and can sometimes develop into end stage renal disease (ESRD), which is caused by mutations in the genes encoding the collagen type IV famil...
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| Publicat a: | Mol Genet Genomic Med |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6625365/ https://ncbi.nlm.nih.gov/pubmed/31144478 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.741 |
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