Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay

BACKGROUND: X‐linked Alport syndrome (XLAS) is a progressive, hereditary glomerular nephritis of variable severity caused by pathogenic COL4A5 variants. Currently, genetic testing is widely used for diagnosing XLAS; however, determining the pathogenicity of variants detected by such analyses can be...

Descripción completa

Detalles Bibliográficos
Autores principales: Horinouchi, Tomoko, Yamamura, Tomohiko, Minamikawa, Shogo, Nagano, China, Sakakibara, Nana, Nakanishi, Koichi, Shima, Yuko, Morisada, Naoya, Ishiko, Shinya, Aoto, Yuya, Nagase, Hiroaki, Takeda, Hiroki, Rossanti, Rini, Ishimori, Shingo, Kaito, Hiroshi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434753/
https://www.ncbi.nlm.nih.gov/pubmed/32543079
http://dx.doi.org/10.1002/mgg3.1342

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7434753/
https://www.ncbi.nlm.nih.gov/pubmed/32543079
http://dx.doi.org/10.1002/mgg3.1342

Ejemplares similares