Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q(10)

Focal segmental glomerulosclerosis (FSGS) and collapsing glomerulopathy are common causes of nephrotic syndrome. Variants in >20 genes, including genes critical for mitochondrial function, have been associated with these podocyte diseases. One such gene, PDSS2, is required for synthesis of the de...

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Main Authors: Gasser, David L., Winkler, Cheryl A., Peng, Min, An, Ping, McKenzie, Louise M., Kirk, Gregory D., Shi, Yuchen, Xie, Letian X., Marbois, Beth N., Clarke, Catherine F., Kopp, Jeffrey B.
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2013
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3798722/
https://ncbi.nlm.nih.gov/pubmed/23926186
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00143.2013
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