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European Journal of Pediatrics, ISSN 0340-6199, 5/2012, Volume 171, Issue 5, pp. 757 - 765
Journal Article
Journal Article
2004, 1. Aufl., Novartis Foundation symposium, ISBN 0470853573, Volume 255, 228
Retinal dystrophies are the major causes of incurable blindness in the Western world. Our insight into their aetiology has improved remarkably over the past... 
Retinal degeneration | Gene therapy | Congresses
eBook
Visual Neuroscience, ISSN 0952-5238, 05/2014, Volume 31, Issue 4-5, pp. 287 - 288
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2018, Volume 1715, pp. 61 - 78
Journal Article
Klinische Monatsblatter fur Augenheilkunde, 03/2017, Volume 234, Issue 3, p. 320
Characteristics of inherited retinal dystrophies include deficiencies in light perception and nervous conduction within the retina, leading to reduced vision... 
Gene Transfer Techniques | Animals | Humans | Retinal Dystrophies - therapy | Eye Diseases, Hereditary - therapy | Treatment Outcome | Evidence-Based Medicine | Retinal Dystrophies - genetics | Genetic Vectors - genetics | Eye Diseases, Hereditary - genetics | Genetic Therapy - methods
Journal Article
Klinische Monatsblatter fur Augenheilkunde, 03/2017, Volume 234, Issue 3, p. 335
Optogenetics refers to the genetic modification of cells to express light-sensitive proteins, which mediate ion flow or secondary signalling cascades upon... 
Animals | Optogenetics - methods | Humans | Retinal Dystrophies - therapy | Evidence-Based Medicine | Retinal Dystrophies - genetics | Genetic Therapy - methods
Journal Article
Klinische Monatsblatter fur Augenheilkunde, 03/2014, Volume 231, Issue 3, p. 210
Treatment possibilities based on specific gene therapy strategies have become reality for a small number of patients with hereditary retinal dystrophies and... 
Retinal Dystrophies - diagnosis | Molecular Diagnostic Techniques - methods | Humans | Retinal Dystrophies - therapy | Retinal Dystrophies - genetics | Genetic Therapy - methods
Journal Article
2004, Novartis Foundation symposium, ISBN 0470853573, Volume 255
Web Resource
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