Comprehensive genetic diagnosis of Japanese patients with severe proteinuria

Numerous disease-causing gene mutations have been identified in proteinuric diseases, such as nephrotic syndrome and glomerulosclerosis. This report describes the results of comprehensive genetic diagnosis of Japanese patients with severe proteinuria. In addition, the report describes the clinical c...

Descripción completa

Detalles Bibliográficos
Autores principales: Nagano, China, Yamamura, Tomohiko, Horinouchi, Tomoko, Aoto, Yuya, Ishiko, Shinya, Sakakibara, Nana, Shima, Yuko, Nakanishi, Koichi, Nagase, Hiroaki, Iijima, Kazumoto, Nozu, Kandai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959278/
https://www.ncbi.nlm.nih.gov/pubmed/31937884
http://dx.doi.org/10.1038/s41598-019-57149-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959278/
https://www.ncbi.nlm.nih.gov/pubmed/31937884
http://dx.doi.org/10.1038/s41598-019-57149-5

Ejemplares similares