A Progressive Autosomal Recessive Cataract Locus Maps to Chromosome 9q13-q22
- 1 March 2001
- journal article
- case report
- Published by Elsevier in American Journal of Human Genetics
- Vol. 68 (3) , 772-777
- https://doi.org/10.1086/318798
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Localization of a Recessive Gene for North American Indian Childhood Cirrhosis to Chromosome Region 16q22—and Identification of a Shared HaplotypeAmerican Journal of Human Genetics, 2000
- Genetic and Environmental Factors in Age-Related Nuclear Cataracts in Monozygotic and Dizygotic TwinsNew England Journal of Medicine, 2000
- The γ-Crystallins and Human Cataracts: A Puzzle Made ClearerAmerican Journal of Human Genetics, 1999
- Connexin46 Mutations in Autosomal Dominant Congenital CataractAmerican Journal of Human Genetics, 1999
- Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in RecombinationAmerican Journal of Human Genetics, 1998
- INVITED EDITORIAL The Genetics of Cataract: Our Vision Becomes ClearerAmerican Journal of Human Genetics, 1998
- A Missense Mutation in the Human Connexin50 Gene (GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1qAmerican Journal of Human Genetics, 1998
- Chromosomal Localization of a New Mouse Lens Opacity Gene (lop18)Genomics, 1996
- Genetic etiology of nuclear cataract: Evidence for a major geneAmerican Journal of Medical Genetics, 1993
- Dominant cataract and recessive specific-locus mutations detected in offspring of procarbazine-treated male miceMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1988