Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

Documenti analoghi

• Adequate use of allele frequencies in Hispanics—a problem elucidated in nephrotic syndrome
  di: Chernin, Gil, et al.
  Pubblicazione: (2009)
• Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS)
  di: Schoeb, Dominik S., et al.
  Pubblicazione: (2010)
• Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of Proteinuria
  di: Ovunc, Bugsu, et al.
  Pubblicazione: (2011)
• Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome
  di: Chernin, Gil, et al.
  Pubblicazione: (2008)
• Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome
  di: Heeringa, Saskia F., et al.
  Pubblicazione: (2008)