Publication: The molecular basis of human retinal and vitreoretinal diseases
The molecular basis of human retinal and vitreoretinal diseases
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Berger, W., Kloeckener-Gruissem, B., & Neidhardt, J. (2010). The molecular basis of human retinal and vitreoretinal diseases. Progress in Retinal and Eye Research, 29(5), 335–375. https://doi.org/10.1016/j.preteyeres.2010.03.004
Abstract
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During the last two to three decades, a large body of work has revealed the molecular basis of many human disorders, including retinal and vitreoretinal degenerations and dysfunctions. Although belonging to the group of orphan diseases, they affect probably more than two million people worldwide. Most excitingly, treatment of a particular form of congenital retinal degeneration is now possible. A major advantage for treatment is the unique structure and accessibility of the eye and its different components, including the vitreous and
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- Berger, W
- Kloeckener-Gruissem, B
- Neidhardt, J
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Citations
Berger, W., Kloeckener-Gruissem, B., & Neidhardt, J. (2010). The molecular basis of human retinal and vitreoretinal diseases. Progress in Retinal and Eye Research, 29(5), 335–375. https://doi.org/10.1016/j.preteyeres.2010.03.004
