# PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/pdzd7-is-a-modifier-of-retinal-disease-and-a-contributor-to-digenic-usher/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Inga Ebermann,Jennifer B. Phillips,Max C. Liebau,Robert K. Koenekoop,Bernhard Schermer,Irma López,Ellen Schäfer,Anne‐Françoise Roux,Claudia Dafinger,Antje Bernd,Eberhart Zrenner,Mireille Claustres,Bernardo Blanco,Gudrun Nürnberg,Peter Nürnberg,Rebecca Ruland,Monte Westerfield,Thomas Benzing,Hanno J. Bolz |
| Citations | 249 |
| DOI | 10.1172/jci39715 |
| Fields | Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology,Neuroscience |
| Open Access | true |
| OA Status | bronze |
| OA URL | http://www.jci.org/articles/view/39715/files/pdf |
| OpenAlex ID | https://openalex.org/W2034223507 |
| PMID | 20440071 |
| Type | article |
| Year | 2010 |

## Paper authors

- [Max C. Liebau](https://scholariq.org/researchers/max-c-liebau/)
- [Thomas Benzing](https://scholariq.org/researchers/thomas-benzing/)

## Paper primary topic

- [Hearing, Cochlea, Tinnitus, Genetics](https://scholariq.org/topics/hearing-cochlea-tinnitus-genetics/)

## Paper topics

- [Hearing, Cochlea, Tinnitus, Genetics](https://scholariq.org/topics/hearing-cochlea-tinnitus-genetics/)
- [Retinal Development and Disorders](https://scholariq.org/topics/retinal-development-and-disorders/)
- [Neutrophil, Myeloperoxidase and Oxidative Mechanisms](https://scholariq.org/topics/neutrophil-myeloperoxidase-and-oxidative-mechanisms/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.