A Major Locus for Autosomal Recessive Retinitis Pigmentosa on 6q, Determined by Homozygosity Mapping of Chromosomal Regions That Contain Gamma-Aminobutyric Acid–Receptor Clusters
- 1 June 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (6) , 1452-1459
- https://doi.org/10.1086/301866
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Intelligent linkage analysis using gene density estimatesNature Genetics, 1997
- Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24Human Molecular Genetics, 1997
- GABAc receptorsTrends in Neurosciences, 1995
- Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6qHuman Molecular Genetics, 1995
- Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6pHuman Molecular Genetics, 1994
- Assignment of a Gene for Autosomal Recessive Retinitis Pigmentosa (RP12) to Chromosome 1q31-q32.1 in an Inbred and Genetically Heterogeneous Disease PopulationGenomics, 1994
- Homozygosity mapping: familiarity breeds debilityNature Genetics, 1993
- Deficiencies in sight with the candidate gene approachNature, 1990
- Quantitative aspects of synaptic ribbon formation in the outer plexiform layer of the developing cat retinaVisual Neuroscience, 1989
- The connections between horizontal cells and photoreceptors in the retina of the cat: Electron microscopy of Golgi preparationsJournal of Comparative Neurology, 1974