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The Value of Clinical Criteria in Identifying Patients with X-Linked Alport Syndrome
BACKGROUND AND OBJECTIVES: Alport syndrome (AS) is a predominantly X-linked hereditary nephritis associated with high-tone, sensorineural deafness and characteristic eye signs. Clinical diagnostic criteria were defined in 1988. Most cases result from mutations in the X-linked collagen gene COL4A5, w...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Nephrology
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3022243/ https://ncbi.nlm.nih.gov/pubmed/20884774 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.00200110 |
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