Genomic Organization of Human CDS2 and Evaluation as a Candidate Gene for Corneal Hereditary Endothelial Dystrophy 2 on Chromosome 20p13
- 30 November 2002
- journal article
- editorial
- Published by Elsevier in Experimental Eye Research
- Vol. 75 (5) , 619-623
- https://doi.org/10.1006/exer.2002.2052
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- The DNA sequence and comparative analysis of human chromosome 20Nature, 2001
- A new pedigree with recessive CHED mapping to the CHED2 locus on 20p13British Journal of Ophthalmology, 2001
- Localization of the Gene for Autosomal Recessive Congenital Hereditary Endothelial Dystrophy (CHED2) to Chromosome 20 by Homozygosity MappingGenomics, 1999
- Identification and Characterization of CDS2, a Mammalian Homolog of theDrosophilaCDP-diacylglycerol Synthase GeneGenomics, 1999
- Isolation and Chromosomal Localization of Two Human CDP-diacylglycerol Synthase (CDS) GenesGenomics, 1998
- Cloning and characterization of human homologue ofDrosophila retinal degeneration B: A candidate gene for degenerative retinal diseasesDevelopmental Genetics, 1997
- Regulation of PLC-mediated signalling in vivo by CDP-diacylglycerol synthaseNature, 1995
- Comparison between posterior polymorphous dystrophy and congenital hereditary endothelial dystrophy of the corneaEye, 1988
- Congenital hereditary corneal oedema of Maumenee: its clinical features, management, and pathology.British Journal of Ophthalmology, 1987
- Hereditary retinal degeneration in Drosophila melanogaster. A mutant defect associated with the phototransduction process.The Journal of general physiology, 1977