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Prof. Dr. Wolfgang Berger - Institute of Medical Molecular Geneticsmore information

Fakultäten » Medizinische Fakultät » Medizinische Molekulargenetik, Institut für » Prof. Dr. Wolfgang Berger

Completed research projects

Project leader Project title
Berger Molecular mechanisms of pathogenesis in Norrie disease and vitreoretinopathies.
Next Generation Sequencing (NGS) for Retinal Diseases
Genetic basis of retinitis pigmentosa (RP) and related retinal degenerations
Molecular signaling in ocular angiogenesis
Congenital stationary night blindness (CSNB)
Berger Kloeckener Cataract and glucosuria due to mutations in SLC16A12
Berger Kloeckener Neidhardt Gene defects in familial and age-related macular degenerations
Berger Mátyás Mutation spectrum in primary congenital lymphedema (PCL1)
Berger Neidhardt Genetic heterogeneity of cone dystrophies
Kloeckener ICF (immunodeficiency, chromosome instability and facial anomalies) syndrome due to mutations in DNMT3B
Neidhardt Gene therapy in retinitis pigmentosa (RP)
Splicing defects in retinal degenerations


Last update 01.02.2016