Associated Papers
PDE6C: Novel Mutations, Atypical Phenotype, and Differences Among Children and Adults.
Daich Varela M et al.
Investigative Ophthalmology & Visual Science, 2020
Modification of the PROM1 disease phenotype by a mutation in ABCA4.
Lee W et al.
Ophthalmic Genetics, 2019
Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia.
Langlo CS et al.
Investigative Ophthalmology & Visual Science, 2016
27479814 (PubMed )
Supplement: i1552-5783-57-10-3984-s04.pdf
Oligocone trichromacy: clinical and molecular genetic investigations.
Andersen MK et al.
Investigative Ophthalmology & Visual Science, 2010
Select a paper to view details