Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndrome

Alport syndrome (AS) is a progressive inherited kidney disease characterized by hearing loss and ocular abnormalities. There are three forms of AS depending on inheritance mode: X-linked Alport syndrome (XLAS), autosomal recessive AS (ARAS), and autosomal dominant AS (ADAS). XLAS is caused by pathog...

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Detalles Bibliográficos
Autores principales: Nozu, Kandai, Takaoka, Yutaka, Kai, Hirofumi, Takasato, Minoru, Yabuuchi, Kensuke, Yamamura, Tomohiko, Horinouchi, Tomoko, Sakakibara, Nana, Ninchoji, Takeshi, Nagano, China, Iijima, Kazumoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Nephrology 2020
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771000/
https://www.ncbi.nlm.nih.gov/pubmed/33214343
http://dx.doi.org/10.23876/j.krcp.20.111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7771000/
https://www.ncbi.nlm.nih.gov/pubmed/33214343
http://dx.doi.org/10.23876/j.krcp.20.111

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