Abca4, mutated in Stargardt disease, is required for structural integrity of cone outer segments

Míreanna comhchosúla

• Identification and functional characterization of ABCA4 gene variants in three patients with Stargardt disease or retinitis pigmentosa
  de réir: Qi Luo, et al.
  Foilsithe / Cruthaithe: (2025-06-01)
• Genotypic Analysis of ABCA4 Coding Sequence in Thai Patients with Stargardt Disease
  de réir: Chinnavuth Vatanashevanopakorn, et al.
  Foilsithe / Cruthaithe: (2024-10-01)
• Identification of Two Novel Mutations in ABCA4 Gene in a Patient With Stargardt Disease
  de réir: Masoumeh Mohebi, et al.
  Foilsithe / Cruthaithe: (2023-10-01)
• Correction of the Splicing Defect Caused by a Recurrent Variant in <i>ABCA4</i> (c.769-784C>T) That Underlies Stargardt Disease
  de réir: Tomasz Z. Tomkiewicz, et al.
  Foilsithe / Cruthaithe: (2022-12-01)
• Interruption of the visual cycle in a novel animal model induces progressive vision loss resembling Stargardts Disease
  de réir: Fabiana Sassone, et al.
  Foilsithe / Cruthaithe: (2024-12-01)