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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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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2980844/ https://ncbi.nlm.nih.gov/pubmed/20023659 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.505 |
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