An inactivating human TRPC6 channel mutation without focal segmental glomerulosclerosis

Transient receptor potential cation channel-6 (TRPC6) gene mutations cause familial focal segmental glomerulosclerosis (FSGS), which is inherited as an autosomal dominant disease. In patients with TRPC6-related FSGS, all mutations map to the N- or C-terminal TRPC6 protein domains. Thus far, the majo...

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Detalles Bibliográficos
Autores principales: Batool, Lilas, Hariharan, Krithika, Xu, Yao, Kaßmann, Mario, Tsvetkov, Dmitry, Gohlke, Björn-Oliver, Kaden, Sylvia, Gossen, Manfred, Nürnberg, Bernd, Kurtz, Andreas, Gollasch, Maik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449997/
https://www.ncbi.nlm.nih.gov/pubmed/37615749
http://dx.doi.org/10.1007/s00018-023-04901-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449997/
https://www.ncbi.nlm.nih.gov/pubmed/37615749
http://dx.doi.org/10.1007/s00018-023-04901-w

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