A Case Report of COL4A5 Gene Mutation Alport Syndrome in 2 Native African Children
Alport syndrome is a heterogeneous genetic disease involving the basement membrane of the glomeruli, inner ear, retina, and lens capsule. It typically manifests as progressive glomerulopathy that frequently results in end-stage renal disease, high-tone sensorineural deafness, and ocular abnormalitie...
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Formato: | article |
Lenguaje: | EN |
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Karger Publishers
2021
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Acceso en línea: | https://doaj.org/article/82dd3681c5114ec091d337bb0b1f3fa9 |
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