Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies

Lignende værker

• CEP290 gene transfer rescues Leber Congenital Amaurosis cellular phenotype
  af: Burnight, E.R., et al.
  Udgivet: (2014)
• Ocular and extra-ocular features of patients with Leber congenital amaurosis and mutations in CEP290
  af: Yzer, Suzanne, et al.
  Udgivet: (2012)
• Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis
  af: den Hollander, Anneke I., et al.
  Udgivet: (2006)
• Visual Acuity Changes in Patients with Leber Congenital Amaurosis (LCA) and Mutations in the CEP290 Gene
  af: McAnany, J. Jason, et al.
  Udgivet: (2013)
• Personalized models reveal mechanistic and therapeutic insights into CEP290-associated Leber congenital amaurosis
  af: McDougald, Devin S., et al.
  Udgivet: (2016)