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Journal Abstract Search

282 related items for PubMed ID: 15500131

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  • 42. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
    Hinkes BG, Mucha B, Vlangos CN, Gbadegesin R, Liu J, Hasselbacher K, Hangan D, Ozaltin F, Zenker M, Hildebrandt F, Arbeitsgemeinschaft für Paediatrische Nephrologie Study Group.
    Pediatrics; 2007 Apr; 119(4):e907-19. PubMed ID: 17371932
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  • 48. Nephrin localizes at the podocyte filtration slit area and is characteristically spliced in the human kidney.
    Holthöfer H, Ahola H, Solin ML, Wang S, Palmen T, Luimula P, Miettinen A, Kerjaschki D.
    Am J Pathol; 1999 Nov; 155(5):1681-7. PubMed ID: 10550324
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  • 53. Novel human pathological mutations. Gene symbol: NPHS1. Disease: congenital nephrotic syndrome, Finnish type.
    Tikhomirov E, Voznesenskaya T, Tsygin A.
    Hum Genet; 2009 Apr; 125(3):334. PubMed ID: 19309778
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  • 60. Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
    Lenkkeri U, Männikkö M, McCready P, Lamerdin J, Gribouval O, Niaudet PM, Antignac C K, Kashtan CE, Homberg C, Olsen A, Kestilä M, Tryggvason K.
    Am J Hum Genet; 1999 Jan; 64(1):51-61. PubMed ID: 9915943
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