Alport autossômica: um estudo de duas famílias norte-rio-grandenses
Alport syndrome (AS) is a genetically rare, heterogeneous and hereditary pathology associated with germline mutations in collagen type IV genes (COL4A3, COL4A4 and COL4A5). Characterized by progressive loss of renal function, hearing and eye damage during early childhood, the progression of the d...
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| Format: | masterThesis |
| Language: | pt_BR |
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Brasil
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| Online Access: | https://repositorio.ufrn.br/jspui/handle/123456789/28765 |
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