Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adults-Reference-Cited by-同舟云学术

Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adults

Published:2006-06-17 Issue:9 Volume:21 Page:2660-2663
ISSN:1460-2385
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:

Author:

Bollée Guillaume,Fakhouri Fadi,Karras Alexandre,Noël Laure-Hélène,Salomon Rémi,Servais Aude,Lesavre Philippe,Morinière Vincent,Antignac Corinne,Hummel Aurélie

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/21/9/2660/7625011/gfl348.pdf

Reference13 articles.

1. Hildebrandt F, Strahm B, Nothwang HG et al. Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. APN Study Group. Arbeitsgemeinschaft fur Padiatrische Nephrologie. Kidney Int1997; 5: 261–269

2. Salomon R, Gubler MC, Antignac C. Nephronophthisis. In: Davidson AM, ed. Oxford Text Book of Clinical Nephrology, 3rd edn. Oxford University Press, Oxford: 2005; 2325–2334

3. Gagnadoux MF, Bacri JL, Broyer M, Habib R. Infantile chronic tubulo-interstitial nephritis with cortical microcysts: variant of nephronophthisis or new disease entity? Pediatr Nephrol1989; 3: 50–55

4. Olbrich H, Fliegauf M, Hoefele J et al. Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis. Nat Genet2003; 34: 455–459

5. Omran H, Fernandez C, Jung M et al. Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree. Am J Hum Genet2000; 66: 118–127

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