Congenital nephrotic syndrome, Finnish type (CNF or NPHS1), is an autosomal recessive disease characterized by massive proteinuria and development of nephrotic syndrome shortly after birth. The disease is most common in Finland, but many patients have been identified in other populations. The diseas
β¦ LIBER β¦
Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS)
β Scribed by Lahdenkari, Anne-Tiina; Kestila, Marjo; Holmberg, Christer; Koskimies, Olli; Jalanko, Hannu
- Book ID
- 109065440
- Publisher
- Nature Publishing Group
- Year
- 2004
- Tongue
- English
- Weight
- 115 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0085-2538
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