Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele

Παρόμοια τεκμήρια

• Retinal Dehydrogenase 12 (RDH12) Mutations in Leber Congenital Amaurosis
  ανά: Perrault, Isabelle, κ.ά.
  Έκδοση: (2004)
• Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis.
  ανά: Perrault, I, κ.ά.
  Έκδοση: (1999)
• Leber Congenital Amaurosis (LCA): Potential for Improvement of Vision
  ανά: Cideciyan, Artur V., κ.ά.
  Έκδοση: (2019)
• The ABCA4 Gene in Autosomal Recessive Cone-Rod Dystrophies
  ανά: Ducroq, Dominique, κ.ά.
  Έκδοση: (2002)
• Treatment Potential for LCA5-Associated Leber Congenital Amaurosis
  ανά: Uyhazi, Katherine E., κ.ά.
  Έκδοση: (2020)