Digenic Inheritance of Early-Onset Glaucoma: CYP1B1, a Potential Modifier Gene
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference72 articles.
1. Recurrent mutations in a single exon encoding the evolutionarily conserved olfactomedin-homology domain of TIGR in familial open-angle glaucoma;Adam;Hum Mol Genet,1997
2. Association of single nucleotide polymorphisms in the interleukin-4 gene and interleukin-4 receptor gene with Crohn's disease in a British population;Aithal;Genes Immun,2001
3. Further evidence for an association of ABCR alleles with age-related macular degeneration;Allikmets;Am J Hum Genet,2000
4. Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A);Alward;N Engl J Med,1998
5. Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene;Alward;Am J Ophthalmol,1998
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