Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis

Ítems similars

• Low prevalence of LRAT mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa
  per: Sweeney, Meredith O., et al.
  Publicat: (2007)
• Homozygosity Mapping in Leber Congenital Amaurosis and Autosomal Recessive Retinitis Pigmentosa in South Indian Families
  per: Srilekha, Sundaramurthy, et al.
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• Rpe65(−/−) and Lrat(−/−) Mice: Comparable Models of Leber Congenital Amaurosis
  per: Fan, Jie, et al.
  Publicat: (2008)
• Disease Course in Patients with Autosomal Recessive Retinitis Pigmentosa due to the USH2A Gene
  per: Sandberg, Michael A., et al.
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• Defining the Residual Vision in Leber Congenital Amaurosis Caused by RPE65 Mutations
  per: Jacobson, Samuel G., et al.
  Publicat: (2008)