A locus for autosomal recessive achromatopsia on human chromosome 8q
- 1 July 1999
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 56 (1), 82-85
- https://doi.org/10.1034/j.1399-0004.1999.560112.x
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Human Rod Monochromacy: Linkage Analysis and Mapping of a Cone Photoreceptor Expressed Candidate Gene on Chromosome 2q11Genomics, 1998
- Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channelNature Genetics, 1998
- Homozygosity Mapping of Achromatopsia to Chromosome 2 Using DNA PoolingHuman Molecular Genetics, 1997
- The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritanceNature Genetics, 1995
- Molecular Genetics of Human Visual PigmentsAnnual Review of Genetics, 1992
- Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences, 1984
- Genetics of Congenital Colour DeficienciesPublished by Springer Science and Business Media LLC ,1972