Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference18 articles.
1. Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type
2. Elevated Frequency and Allelic Heterogeneity of Congenital Nephrotic Syndrome, Finnish Type, in the Old Order Mennonites
3. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
4. Maternal serum alpha-fetoprotein levels in congenital nephrotic syndrome carrier pregnancies
5. Maternal serum alpha-fetoprotein levels in congenital nephrosis
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