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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Vydáno v:Kidney Res Clin Pract
Hlavní autoři: Nozu, Kandai, Takaoka, Yutaka, Kai, Hirofumi, Takasato, Minoru, Yabuuchi, Kensuke, Yamamura, Tomohiko, Horinouchi, Tomoko, Sakakibara, Nana, Ninchoji, Takeshi, Nagano, China, Iijima, Kazumoto
Médium: Artigo
Jazyk:Inglês
Vydáno: Korean Society of Nephrology 2020
Témata:
Review Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7771000/
https://ncbi.nlm.nih.gov/pubmed/33214343
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.23876/j.krcp.20.111
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