Correction: Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions

Ítems similars

• Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions
  per: Kumaran, Neruban, et al.
  Publicat: (2017)
• Molecular Screening of 43 Brazilian Families Diagnosed with Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy
  per: Porto, Fernanda B. O., et al.
  Publicat: (2017)
• Pathogenicity Reclassification of RPE65 Missense Variants Related to Leber Congenital Amaurosis and Early-Onset Retinal Dystrophy
  per: Motta, Fabiana L., et al.
  Publicat: (2019)
• A syndrome of congenital retinal dystrophy and saccade palsy--a subset of Leber's amaurosis.
  per: Moore, A. T., et al.
  Publicat: (1984)
• An Update on Gene Therapy for Inherited Retinal Dystrophy: Experience in Leber Congenital Amaurosis Clinical Trials
  per: Chiu, Wei, et al.
  Publicat: (2021)