COL4A6 is dispensable for autosomal recessive Alport syndrome

Alport syndrome is caused by mutations in the genes encoding α3, α4, or α5 (IV) chains. Unlike X-linked Alport mice, α5 and α6 (IV) chains are detected in the glomerular basement membrane of autosomal recessive Alport mice, however, the significance of this finding remains to be investigated. We the...

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Detalles Bibliográficos
Autores principales: Murata, Tomohiro, Katayama, Kan, Oohashi, Toshitaka, Jahnukainen, Timo, Yonezawa, Tomoko, Sado, Yoshikazu, Ishikawa, Eiji, Nomura, Shinsuke, Tryggvason, Karl, Ito, Masaaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932521/
https://www.ncbi.nlm.nih.gov/pubmed/27377778
http://dx.doi.org/10.1038/srep29450

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932521/
https://www.ncbi.nlm.nih.gov/pubmed/27377778
http://dx.doi.org/10.1038/srep29450

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