Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. (Q41696457)
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scientific article published on 6 July 2017
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. |
scientific article published on 6 July 2017 |
Statements
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome (English)
Christine Neuhaus
Tobias Eisenberger
Christian Decker
Sandra Nagl
Cornelia Blank
Markus Pfister
Cornelie Müller-Hofstede
Raoul Heller
Bodo Beck
Klaus Rüther
Diana Mitter
Klaus Rohrschneider
Ute Steinhauer
Heike M Korbmacher
Dagmar Huhle
Solaf M Elsayed
Hesham M Taha
Heidi Stöhr
Markus Preising
Susanne Markus
Fabian Moeller
Birgit Lorenz
Kerstin Nagel-Wolfrum
Arif O Khan
Ingo Kennerknecht
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