Disease Course in Patients with Autosomal Recessive Retinitis Pigmentosa due to the USH2A Gene

פריטים דומים

• Low prevalence of LRAT mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa
  מאת: Sweeney, Meredith O., et al.
  יצא לאור: (2007)
• A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa
  מאת: den Hollander, Anneke I., et al.
  יצא לאור: (2008)
• Association of Vitamin A Supplementation With Disease Course in Children With Retinitis Pigmentosa
  מאת: Berson, Eliot L., et al.
  יצא לאור: (2018)
• Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa
  מאת: McGee, Terri L., et al.
  יצא לאור: (2010)
• Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis
  מאת: Morimura, Hiroyuki, et al.
  יצא לאור: (1998)