Christiana Marchese

We don’t have enough information about this author to calculate their statistics. If you think this is an error let us know.
Learn More
By screening patients with autosomal dominant retinitis pigmentosa for mutations in the rhodopsin gene, two deletions (8bp and 1bp) have been identified in exon 5; these deletions cause a shift in the reading frame. The predicted proteins should be radically altered with translation continuing past the normal stop signal and resulting in a rhodopsin(More)
  • 1