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J-GLOBAL ID:201302200241572505   Reference number:13A0035010

Nonfunction of the ECT2 gene may cause renal tubulointerstitial injury leading to focal segmental glomerulosclerosis

ECT2遺伝子の非機能は腎尿細管間質損傷を生じ,巣状分節性糸球体硬化症を生じる
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Volume: 16  Issue:Page: 875-882  Publication year: Dec. 2012 
JST Material Number: L3173A  ISSN: 1342-1751  Document type: Article
Article type: 原著論文  Country of issue: Germany, Federal Republic of (DEU)  Language: ENGLISH (EN)
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Clinical medicine on urogenital system in general  ,  Molecular genetics in general 
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Reference (23):
  • KIFFEL, J. Focal segmental glomerulosclerosis and chronic kidney disease in pediatric patients. Adv Chronic Kidney Dis. 2011, 18, 332-338
  • GBADEGESIN, R. Pathogenesis and therapy of focal segmental glomerulosclerosis : an update. Pediatr Nephrol. 2011, 26, 1001-1015
  • COPELOVITCH, L. Hpothesis : Dent disease is an underrecognized cause of focal glomerulosclerosis. Clin J Am Soc Nephrol. 2007, 2, 914-918
  • KANEKO, K. Focal segmental glomerulosclerosis in a boy wish Dent-2 disease. Pediatr Nephrol. 2010, 25, 781-782
  • TADA, M. Histopathological evidence of poor prognosis in patients with vesicoureteral reflux. Pediatr Nephrol. 2001, 16, 482-487
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