Glomerular Basement Membrane Protein Expression and the Diagnosis and Prognosis of Autosomal Dominant Alport Syndrome

Alport syndrome is a hereditary glomerular nephritis associated with hearing loss and eye abnormalities and is classified as X-linked Alport syndrome, autosomal recessive Alport syndrome, and autosomal dominant Alport syndrome. Autosomal dominant Alport syndrome is caused by a mutation in the gene e...

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Detalles Bibliográficos
Autores principales: Akihisa, Taro, Sato, Masayo, Wakayama, Yoshie, Taneda, Sekiko, Horita, Shigeru, Hirose, Orie, Makabe, Shiho, Kataoka, Hiroshi, Mori, Takayasu, Sohara, Eisei, Uchida, Shinichi, Nitta, Kosaku, Mochizuki, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7380416/
https://www.ncbi.nlm.nih.gov/pubmed/32734219
http://dx.doi.org/10.1016/j.xkme.2019.06.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7380416/
https://www.ncbi.nlm.nih.gov/pubmed/32734219
http://dx.doi.org/10.1016/j.xkme.2019.06.007

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