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

RPE65 is a protein of unknown function expressed specifically by the retinal pigment epithelium. We examined all 14 exons of this gene in 147 unrelated patients with autosomal recessive retinitis pigmentosa (RP), in 15 patients with isolate RP, and in 45 patients with Leber congenital amaurosis (LCA...

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Hlavní autoři: Morimura, Hiroyuki, Fishman, Gerald A., Grover, Sandeep A., Fulton, Anne B., Berson, Eliot L., Dryja, Thaddeus P.
Médium: Artigo
Jazyk:Inglês
Vydáno: The National Academy of Sciences 1998
Témata:
Biological Sciences
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC19699/
https://ncbi.nlm.nih.gov/pubmed/9501220
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