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Paper Details

Focal segmental glomerulosclerosis with a mutation in the <i>mitochondrially encoded NADH dehydrogenase 5</i> gene: A case report.
Mol Genet Metab Rep
0
2023
AiDIVs, Complex I, FSGS, Focal segmental glomerulosclerosis, GSECs, NADH, NADH dehydrogenase 5, ND5, ReCPos, cytoplasm, granular swollen epithelial cells, m.13513 G, mitochondrial diseases, mitochondrial oxidative phosphorylation (OXPHOS) disorder, patient, peripheral mononuclear blood cells, podocyte, podocytes, proteinuria, red, red-coloured podocytes, renal dysfunction, tubular cells, urine sediment cells, vascular smooth muscle cells, woman
Author NameAffiliation
Yasushi OkazakiIntractable Disease Research Center, Graduate School of Medicine, Juntendo University
Yasushi OkazakiIntractable Disease Research Center, Graduate School of Medicine, Juntendo University
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Datasets

Release 1.2