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A family case of X-linked Alport syndrome patients with a novel variant in COL4A5
We herein report 2 Japanese patients with X-linked Alport syndrome (XLAS), with a novel variant in COL4A5. Patient 1 was a 16-year-old Japanese girl with a history of microscopic hematuria, without proteinuria, renal dysfunction, deafness, or ocular abnormalities. At 13 years of age, renal biopsy wa...
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| Publicado no: | CEN Case Rep |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Singapore
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6450996/ https://ncbi.nlm.nih.gov/pubmed/30293132 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-018-0368-4 |
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