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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Kidney Int Rep |
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| Prif Awduron: | , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Elsevier
2018
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| Pynciau: | |
| Mynediad Ar-lein: | 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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