University of Münster
CRIS@UM
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Cornelie Barbara Julie Müller-Hofstede

Current affiliations

  • Institute of Human Genetics

Publications

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
Neuhaus C., Eisenberger T., Decker C., Nagl S., Blank C., Pfister M., Kennerknecht I., Müller-Hofstede C., Charbel Issa P., Heller R., Beck B., Rüther K., Mitter D., Rohrschneider K., Steinhauer U., Korbmacher H., Huhle D., Elsayed S., Taha H., Baig S., Stöhr H., Preising M., Markus S., Moeller F., Lorenz B., Nagel-Wolfrum K., Khan A., Bolz H. (2017)
In: ((Bitte Journal prüfen)), 5(5).
Research article (journal)