Genome-wide association study in RPGRIP1(−/−) dogs identifies a modifier locus that determines the onset of retinal degeneration

Eitemau Tebyg

• Phenotypic variation and genotype-phenotype discordance in canine cone-rod dystrophy with an RPGRIP1 mutation
  gan: Miyadera, Keiko, et al.
  Cyhoeddwyd: (2009)
• A Frameshift Mutation in Golden Retriever Dogs with Progressive Retinal Atrophy Endorses SLC4A3 as a Candidate Gene for Human Retinal Degenerations
  gan: Downs, Louise M., et al.
  Cyhoeddwyd: (2011)
• A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies
  gan: Khanna, Hemant, et al.
  Cyhoeddwyd: (2009)
• Inherited retinal diseases in dogs: advances in gene/mutation discovery
  gan: Miyadera, Keiko
  Cyhoeddwyd: (2014)
• Assessment of Hereditary Retinal Degeneration in the English Springer Spaniel Dog and Disease Relationship to an RPGRIP1 Mutation
  gan: Narfström, Kristina, et al.
  Cyhoeddwyd: (2012)