A review of clinical characteristics and genetic backgrounds in Alport syndrome

Alport syndrome (AS) is a progressive hereditary renal disease that is characterized by sensorineural hearing loss and ocular abnormalities. It is divided into three modes of inheritance, namely, X-linked Alport syndrome (XLAS), autosomal recessive AS (ARAS), and autosomal dominant AS (ADAS). XLAS i...

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Detalles Bibliográficos
Autores principales: Nozu, Kandai, Nakanishi, Koichi, Abe, Yoshifusa, Udagawa, Tomohiro, Okada, Shinichi, Okamoto, Takayuki, Kaito, Hiroshi, Kanemoto, Katsuyoshi, Kobayashi, Anna, Tanaka, Eriko, Tanaka, Kazuki, Hama, Taketsugu, Fujimaru, Rika, Miwa, Saori, Yamamura, Tomohiko, Yamamura, Natsusmi, Horinouchi, Tomoko, Minamikawa, Shogo, Nagata, Michio, Iijima, Kazumoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2018
Materias:
Invited Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510800/
https://www.ncbi.nlm.nih.gov/pubmed/30128941
http://dx.doi.org/10.1007/s10157-018-1629-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510800/
https://www.ncbi.nlm.nih.gov/pubmed/30128941
http://dx.doi.org/10.1007/s10157-018-1629-4

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