Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients-Reference-Cited by-同舟云学术

Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients

Published:2000-09 Issue:3 Volume:58 Page:972-980
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Patrakka Jaakko,Kestilä Marjo,Wartiovaara Jorma,Ruotsalainen Vesa,Tissari Päivi,Lenkkeri Ulla,Männikkö Minna,Visapää Ilona,Holmberg Christer,Rapola Juhani,Tryggvason Karl,Jalanko Hannu

Publisher

Elsevier BV

Subject

Nephrology

Reference23 articles.

1. Congenital nephrotic syndrome,;Holmberg,1999

2. Nephrotic syndrome in newborn and young infants;Hallman;Ann Pediatr Fenn,1956

3. Hereditary in the congenital nephrotic syndrome;Norio;Ann Pediatr Fenn,1966

4. Congenital nephrotic syndrome of the Finnish type: Linkage to the locus in a non-Finnish population;Fuschuber;Pediatr Nephrol,1996

5. Congenital nephrotic syndrome of Finnish type: Study of 75 cases;Huttunen;Arch Dis Child,1976

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