A Novel CLCN5 Mutation Associated With Focal Segmental Glomerulosclerosis and Podocyte Injury

INTRODUCTION: Tubular dysfunction is characteristic of Dent’s disease; however, focal segmental glomerulosclerosis (FSGS) can also be present. Glomerulosclerosis could be secondary to tubular injury, but it remains uncertain whether the CLCN5 gene, which encodes an endosomal chloride and/or hydrogen...

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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Kidney Int Rep
Päätekijät: Solanki, Ashish K., Arif, Ehtesham, Morinelli, Thomas, Wilson, Robert C., Hardiman, Gary, Deng, Peifeng, Arthur, John M., Velez, Juan CQ, Nihalani, Deepak, Janech, Michael G., Budisavljevic, Milos N.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2018
Aiheet:
Translational Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6224352/
https://ncbi.nlm.nih.gov/pubmed/30426109
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ekir.2018.06.003
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