Deciphering the pathogenesis of the COL4‐related hematuric nephritis: A genotype/phenotype study

BACKGROUND: Alport syndrome (ATS) is a hereditary progressive hematuric nephropathy associated with sensorineural deafness and ocular abnormalities, which is caused by mutations in the COL4A5 gene (X‐linked ATS) and in two autosomal genes, COL4A4 and COL4A3, responsible of both recessive ATS and, wh...

Descripción completa

Detalles Bibliográficos
Autores principales: Uliana, Vera, Sebastio, Paola, Riva, Matteo, Carli, Diana, Ruberto, Claudio, Bianchi, Laura, Graziano, Claudio, Capelli, Irene, Faletra, Flavio, Pillon, Roberto, Mattina, Teresa, Sensi, Alberto, Bonatti, Francesco, Percesepe, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077073/
https://www.ncbi.nlm.nih.gov/pubmed/33369211
http://dx.doi.org/10.1002/mgg3.1576

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077073/
https://www.ncbi.nlm.nih.gov/pubmed/33369211
http://dx.doi.org/10.1002/mgg3.1576

Ejemplares similares