Renal disease with OCRL1 mutations: Dent-2 or Lowe syndrome?

Ítems similars

• Dent Disease with Mutations in OCRL1
  per: Hoopes, Richard R., et al.
  Publicat: (2005)
• Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease
  per: Suarez-Artiles, Lorena, et al.
  Publicat: (2018)
• Novel OCRL mutations in patients with Dent-2 disease
  per: Böckenhauer, Detlef, et al.
  Publicat: (2012)
• Mouse Model for Lowe Syndrome/Dent Disease 2 Renal Tubulopathy
  per: Bothwell, Susan P., et al.
  Publicat: (2011)
• Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome.
  per: Lin, T, et al.
  Publicat: (1997)