Contribution of post-receporal cells to the cone a-wave of the human electroretinogram in congenital stationary night blindness and autoimmune-like retinopathy

Author:

Bradshaw Keith,Hanitzsch Renate

Publisher

Elsevier BV

Subject

Sensory Systems,Ophthalmology

Reference53 articles.

1. Autoantibodies against retinal proteins in paraneoplastic and autoimmune retinopathy;Adamus;BMC Ophthalmology,2004

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3. Genotype–phenotype correlation in British families with X-linked congenital stationary night blindness;Allen;British Journal of Ophthalmology,2003

4. The negative ERG: Clinical phenotypes and disease mechanisms of inner retinal dysfunction;Audo;Survey of Ophthalmology,2008

5. Bech-Hansen, N., Loucks, C., Beaulieu, C., Weleber, R., Rosenberg, T., Brennan, R., et al. (2010). Mutation analysis in a cohort of CSNB patients: Novel mutations in TRPM1 gene. Investigative Ophthalmology & Visual Science 51 [E–Abstract 4129].

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