An ADAM9 mutation in canine cone-rod dystrophy 3 establishes homology with human cone-rod dystrophy 9 Academic Article uri icon

Overview

MeSH Major

  • ADAM Proteins
  • Dog Diseases
  • Mutation
  • Retinitis Pigmentosa

abstract

  • Identification of this ADAM9 deletion in crd3-affected dogs establishes this canine disease as orthologous to CORD9 in humans, and offers opportunities for further characterization of the disease process, and potential for genetic therapeutic intervention.

publication date

  • August 20, 2010

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC2925905

PubMed ID

  • 20806078

Additional Document Info

start page

  • 1549

end page

  • 69

volume

  • 16