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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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Detalles Bibliográficos
Autores principales:	Oduware, Emmanuel, Iduoriyekemwen, Nosakhare Joyce, Ibadin, Michael, Aikhionbare, Henry
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	S. Karger AG 2021
Materias:	Case Series
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613556/ https://www.ncbi.nlm.nih.gov/pubmed/34901198 http://dx.doi.org/10.1159/000519076

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