A third locus for dominant optic atrophy on chromosome 22q

Ítems similars

• Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele
  per: Perrault, I, et al.
  Publicat: (2003)
• The ABCA4 Gene in Autosomal Recessive Cone-Rod Dystrophies
  per: Ducroq, Dominique, et al.
  Publicat: (2002)
• Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus
  per: Rozet, J., et al.
  Publicat: (1999)
• Retinal Dehydrogenase 12 (RDH12) Mutations in Leber Congenital Amaurosis
  per: Perrault, Isabelle, et al.
  Publicat: (2004)
• Dominant X linked retinitis pigmentosa is frequently accounted for by truncating mutations in exon ORF15 of the RPGR gene
  per: Rozet, J, et al.
  Publicat: (2002)