Characterization of the Gene for HRG4 (UNC119), a Novel Photoreceptor Synaptic Protein Homologous to Unc-119
Open Access
- 1 May 1999
- journal article
- research article
- Published by Elsevier BV in Genomics
- Vol. 57 (3), 446-450
- https://doi.org/10.1006/geno.1999.5791
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Cloning of the cDNA for a Novel Photoreceptor ProteinOnline Journal of Public Health Informatics, 1996
- An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17qHuman Molecular Genetics, 1995
- A homozygous 1–base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in JapaneseNature Genetics, 1995
- Ca2+-dependent Interaction of Recoverin with Rhodopsin KinaseOnline Journal of Public Health Informatics, 1995
- A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17Human Molecular Genetics, 1994
- A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosaNature, 1991
- Proceedings of the Second International Workshop on Human Chromosome 17 Mapping 1991Cytogenetic and Genome Research, 1991
- Retinal degeneration in the rd mouse is caused by a defect in the β subunit of rod cGMP-phosphodiesteraseNature, 1990
- A point mutation of the rhodopsin gene in one form of retinitis pigmentosaNature, 1990
- Organization and Expression of Eucaryotic Split Genes Coding for ProteinsAnnual Review of Biochemistry, 1981