Mutations in the formin protein INF2 cause focal segmental glomerulosclerosis

Focal segmental glomerulosclerosis (FSGS) is a pattern of kidney injury observed either as an idiopathic finding or as a consequence of underlying systemic conditions. Several genes have been identified which, when mutated, lead to inherited FSGS and/or the nephrotic syndrome. These findings have ac...

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Detalles Bibliográficos
Autores principales: Brown, Elizabeth J., Schlöndorff, Johannes S., Becker, Daniel J., Tsukaguchi, Hiroyasu, Uscinski, Andrea L., Higgs, Henry N., Henderson, Joel M., Pollak, Martin R.
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980844/
https://www.ncbi.nlm.nih.gov/pubmed/20023659
http://dx.doi.org/10.1038/ng.505

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980844/
https://www.ncbi.nlm.nih.gov/pubmed/20023659
http://dx.doi.org/10.1038/ng.505

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