The ABCA4 Gene in Autosomal Recessive Cone-Rod Dystrophies

Παρόμοια τεκμήρια

• Retinal Dehydrogenase 12 (RDH12) Mutations in Leber Congenital Amaurosis
  ανά: Perrault, Isabelle, κ.ά.
  Έκδοση: (2004)
• ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies
  ανά: Kitiratschky, Veronique B.D., κ.ά.
  Έκδοση: (2008)
• Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele
  ανά: Perrault, I, κ.ά.
  Έκδοση: (2003)
• A third locus for dominant optic atrophy on chromosome 22q
  ανά: Barbet, F, κ.ά.
  Έκδοση: (2005)
• A retGC-1 mutation in autosomal dominant cone-rod dystrophy.
  ανά: Perrault, I, κ.ά.
  Έκδοση: (1998)