RESPIRATORY CHAIN DEFICIENCY PRESENTING AS DIFFUSE MESANGIAL SCLEROSIS WITH NPHS3 MUTATION

Antzeko izenburuak

• Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome
  nork: Heeringa, Saskia F., et al.
  Argitaratua: (2008)
• Mutation Analysis of NPHS1 in a Worldwide Cohort of Congenital Nephrotic Syndrome Patients
  nork: Ovunc, Bugsu, et al.
  Argitaratua: (2012)
• Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome
  nork: Chernin, Gil, et al.
  Argitaratua: (2008)
• Diffuse mesangial sclerosis – Report of two cases
  nork: Vankalakunti, M., et al.
  Argitaratua: (2012)
• Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS)
  nork: Schoeb, Dominik S., et al.
  Argitaratua: (2010)