Low prevalence of LRAT mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa

Gelijkaardige items

• Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis
  door: Morimura, Hiroyuki, et al.
  Gepubliceerd in: (1998)
• Disease Course in Patients with Autosomal Recessive Retinitis Pigmentosa due to the USH2A Gene
  door: Sandberg, Michael A., et al.
  Gepubliceerd in: (2008)
• A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa
  door: den Hollander, Anneke I., et al.
  Gepubliceerd in: (2008)
• Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families
  door: Srilekha, Sundaramurthy, et al.
  Gepubliceerd in: (2015)
• Null RPGRIP1 Alleles in Patients with Leber Congenital Amaurosis
  door: Dryja, Thaddeus P., et al.
  Gepubliceerd in: (2001)