Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis

Mutations in the inverted formin 2 gene (INF2) have recently been identified as the most common cause of autosomal dominant focal and segmental glomerulosclerosis (FSGS). In order to quantify the contribution of various genes contributing to FSGS, we sequenced INF2 where all mutations have previousl...

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Detalles Bibliográficos
Autores principales: Barua, Moumita, Brown, Elizabeth J., Charoonratana, Victoria T., Genovese, Giulio, Sun, Hua, Pollak, Martin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647680/
https://www.ncbi.nlm.nih.gov/pubmed/23014460
http://dx.doi.org/10.1038/ki.2012.349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647680/
https://www.ncbi.nlm.nih.gov/pubmed/23014460
http://dx.doi.org/10.1038/ki.2012.349

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