Central Visual Function and Genotype–Phenotype Correlations in <i>PDE6A</i>-Associated Retinitis Pigmentosa-Reference-Cited by-同舟云学术

Central Visual Function and Genotype–Phenotype Correlations in PDE6A-Associated Retinitis Pigmentosa

Published:2022-05-09 Issue:5 Volume:63 Page:9
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Kuehlewein Laura¹²,Straßer Torsten¹²,Blumenstock Gunnar³,Stingl Katarina¹,Fischer M. Dominik²,Wilhelm Barbara⁴,Zrenner Eberhart²⁵,Wissinger Bernd⁶,Kohl Susanne⁶,Weisschuh Nicole⁶,Zobor Ditta²⁷,

Affiliation:

1. University Eye Hospital, Centre for Ophthalmology, Eberhard Karls University of Tübingen, Tübingen, Germany

2. Institute for Ophthalmic Research, Centre for Ophthalmology, Eberhard Karls University of Tübingen, Tübingen, Germany

3. Department of Clinical Epidemiology, Eberhard Karls University of Tübingen, Tübingen, Germany

4. STZ eyetrial at the Centre for Ophthalmology, Eberhard Karls University of Tübingen, Tübingen, Germany

5. Werner Reichardt Centre for Integrative Neuroscience, Eberhard Karls University of Tübingen, Tübingen, Germany

6. Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, Eberhard Karls University of Tübingen, Tübingen, Germany

7. Department of Ophthalmology, Semmelweis University, Budapest, Hungary

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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4. Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase;Huang;Nat Genet,1995

5. cGMP signaling in vertebrate retinal photoreceptor cells;Zhang;Front Biosci,2005

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