De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis

This publication has 14 references indexed in Scilit:

• Mutations in the Cone-Rod Homeobox Gene Are Associated with the Cone-Rod Dystrophy Photoreceptor Degeneration
  Neuron, 1997
• Crx, a Novel otx-like Homeobox Gene, Shows Photoreceptor-Specific Expression and Regulates Photoreceptor Differentiation
  Cell, 1997
• Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene () Essential for Maintenance of the Photoreceptor
  Cell, 1997
• Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy
  Nature Genetics, 1997
• Mutations in RPE65 cause Leber's congenital amaurosis
  Nature Genetics, 1997
• Retinal–specific guanylate cyclase gene mutations in Leber's congenital amaurosis
  Nature Genetics, 1996
• Vision in Leber Congenital Amaurosis
  Archives of Ophthalmology (1950), 1996
• The Natural History of Leber's Congenital Amoaurosis
  Ophthalmology, 1992
• Leber's Congenital Amaurosis
  Archives of Ophthalmology (1950), 1978
• Ueber Retinitis pigmentosa und angeborene Amaurose
  Graefe's Archive for Clinical and Experimental Ophthalmology, 1869