Alport Syndrome: Clinical Spectrum and Therapeutic Advances

Alport syndrome is a hereditary disorder characterized by kidney disease, ocular abnormalities, and sensorineural hearing loss. Work in understanding the cause of Alport syndrome and the molecular composition of the glomerular basement membrane ultimately led to the identification of COL4A3, COL4A4...

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Detalles Bibliográficos
Autores principales: Gregorio, Vanessa De, Caparali, Emine Bilge, Shojaei, Azadeh, Ricardo, Samantha, Barua, Moumita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131117/
https://www.ncbi.nlm.nih.gov/pubmed/37122389
http://dx.doi.org/10.1016/j.xkme.2023.100631

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131117/
https://www.ncbi.nlm.nih.gov/pubmed/37122389
http://dx.doi.org/10.1016/j.xkme.2023.100631

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