* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download New gene link to Glaucoma
Genetic testing wikipedia , lookup
Epigenetics of diabetes Type 2 wikipedia , lookup
Koinophilia wikipedia , lookup
Gene expression programming wikipedia , lookup
Genetic engineering wikipedia , lookup
Genomic imprinting wikipedia , lookup
Artificial gene synthesis wikipedia , lookup
Heritability of IQ wikipedia , lookup
Ridge (biology) wikipedia , lookup
Epigenetics of human development wikipedia , lookup
Quantitative trait locus wikipedia , lookup
Site-specific recombinase technology wikipedia , lookup
History of genetic engineering wikipedia , lookup
Minimal genome wikipedia , lookup
Fetal origins hypothesis wikipedia , lookup
Genome evolution wikipedia , lookup
Behavioural genetics wikipedia , lookup
Neuronal ceroid lipofuscinosis wikipedia , lookup
Population genetics wikipedia , lookup
Medical genetics wikipedia , lookup
Frameshift mutation wikipedia , lookup
Gene expression profiling wikipedia , lookup
Biology and consumer behaviour wikipedia , lookup
Epigenetics of neurodegenerative diseases wikipedia , lookup
Oncogenomics wikipedia , lookup
Designer baby wikipedia , lookup
Point mutation wikipedia , lookup
Nutriepigenomics wikipedia , lookup
Genome (book) wikipedia , lookup
Media Statement Thursday, January 14, 2016 New genes linked to world’s leading cause of irreversible blindness Glaucoma is the leading cause of irreversible blindness worldwide, affecting more than 65 million people. Prof David Mackey, genetic researcher and Managing Director of the Lions Eye Institute, is a member of the consortium that have identified three new gene mutations associated with an increased susceptibility to primary open-angle glaucoma (POAG); the most common form of the disease. Their findings were published this week in Nature Genetics. The researchers performed a meta-analysis of genome-wide association studies from the United States, Europe, Singapore, Australia and New Zealand. They found that people with the mutations in one or more of these three genes had an increased risk of developing POAG. The results also identify new pathways underlying POAG susceptibility, which in turn could offer new opportunities for preventative therapies. Media Contact: Kari Legge – [email protected] / 08 9381 0823