Electrophysiological analysis of visual function in mutant mice.
- 1 January 2003
- journal article
- review article
- Published by Springer Nature in Documenta Ophthalmologica
- Vol. 107 (1) , 13-35
- https://doi.org/10.1023/a:1024448314608
Abstract
No abstract availableKeywords
This publication has 96 references indexed in Scilit:
- Missense mutation in the gene encoding the α subunit of rod transducin in the Nougaret form of congenital stationary night blindnessNature Genetics, 1996
- Probable exclusion of the cortexin-encoding gene as a candidate for mouse neurological mutants: nervous, tottering and motor neuron degenerationGene, 1996
- A candidate gene for the mouse mutation tubbyNature, 1996
- An electrode to record the mouse cornea electroretinogramDocumenta Ophthalmologica, 1995
- Defective myosin VIIA gene responsible for Usher syndrome type IBNature, 1995
- Rhodopsin mutation G90D and a molecular mechanism for congenital night blindnessNature, 1994
- Electro-oculogram changes in patients with ocular hypertension and primary open-angle glaucomaDocumenta Ophthalmologica, 1993
- Effects of the murine mutation ?nervous? on neurons in cerebellum and dorsal cochlear nucleusJournal of Neurocytology, 1988
- Spectral sensitivity of human cone photoreceptorsNature, 1987
- Absence of receptor outer segments in the retina of rds mutant miceNeuroscience Letters, 1981