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Genomatix Software GmbH Bayerstr. 85a 80336 München, Germany http://www.genomatix.de
Contact Mr Klaus May +49 89 5997660
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Genomatix Software GmbH

Transcription Factor Scan Identifies Genetic Cause for Inherited Blindness

A multinational team effort of Regensburg's Institute of Human Genetics, Washington University in St. Louis, other partners, and Genomatix elucidated a transcriptional network in photoreceptors and thereby identified a novel retinal disease gene

(PresseBox) (München, )
Retinitis pigmentosa is an inherited eye disorder characterized by progressive loss of vision that in many instances leads to legal blindness at the end stage.

In a ChIP-Seq based approach, the researchers identified a key regulatory role of the transcription factor Crx (Cone-rod homeobox) in the expression of retina-specific genes and thus described an important genetic basis for visual perception. In-depth analysis of Crx mediated regulation in photoreceptors with latest technology provided by Genomatix lead then to the identification of nonsense mutations in the human FAM161A gene, which are responsible for RP28-associated recessive retinitis pigmentosa.

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The publisher indicated in each case (see company info by clicking on image/title or company info in the right-hand column) is solely responsible for the stories above, the event or job offer shown and for the image and audio material displayed. As a rule, the publisher is also the author of the texts and the attached image, audio and information material. The use of information published here is generally free of charge for personal information and editorial processing. Please clarify any copyright issues with the stated publisher before further use. In case of publication, please send a specimen copy to service@pressebox.de.