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Letters to the Journal

Novel homozygous mutation in the SPATA7 gene causes autosomal recessive retinal degeneration in a consanguineous German family

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Acknowledgment

Diagnostic genetic testing was performed by CeGat GmbH, Tübingen, Germany. We are grateful to the patients for their participation.

Declaration of interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.

Funding

The study was supported by a ProRetina grant (Projekt Pro-Re/Projekt/Zobor.1-2016) for BF, SK, and DZ.

Additional information

Funding

The study was supported by a ProRetina grant (Projekt Pro-Re/Projekt/Zobor.1-2016) for BF, SK, and DZ.

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