Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone–rod dystrophy

Podobne zapisy

• A retGC-1 mutation in autosomal dominant cone-rod dystrophy.
  od: Perrault, I, i wsp.
  Wydane: (1998)
• Cloning and expression of a second photoreceptor-specific membrane retina guanylyl cyclase (RetGC), RetGC-2.
  od: Lowe, D G, i wsp.
  Wydane: (1995)
• Two amino acid substitutions convert a guanylyl cyclase, RetGC-1, into an adenylyl cyclase
  od: Tucker, Chandra L., i wsp.
  Wydane: (1998)
• AAV-Mediated Gene Therapy in the Guanylate Cyclase (RetGC1/RetGC2) Double Knockout Mouse Model of Leber Congenital Amaurosis
  od: Boye, Sanford L., i wsp.
  Wydane: (2013)
• Autosomal dominant cone-rod dystrophy with negative electroretinogram.
  od: Fujii, N, i wsp.
  Wydane: (1995)