Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial Intelligence

Benzer Materyaller

• Transient pupillary light reflex in CEP290- or NPHP5- associated Leber congenital amaurosis: Latency as a potential outcome measure of cone function
  Yazar:: Krishnan, Arun K., ve diğerleri
  Baskı/Yayın Bilgisi: (2020)
• Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis
  Yazar:: den Hollander, Anneke I., ve diğerleri
  Baskı/Yayın Bilgisi: (2006)
• Natural History of Cone Disease in the Murine Model of Leber Congenital Amaurosis Due to CEP290 Mutation: Determining the Timing and Expectation of Therapy
  Yazar:: Boye, Shannon E., ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy
  Yazar:: Cideciyan, Artur V., ve diğerleri
  Baskı/Yayın Bilgisi: (2011)
• Leber Congenital Amaurosis Due to GUCY2D Mutations: Longitudinal Analysis of Retinal Structure and Visual Function
  Yazar:: Jacobson, Samuel G., ve diğerleri
  Baskı/Yayın Bilgisi: (2021)