Search

Author/Creator Preising, Markus

2. 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. Issue 5 (6th July 2017)

Authors:
Neuhaus, Christine; Eisenberger, Tobias; Decker, Christian; Nagl, Sandra; Blank, Cornelia; Pfister, Markus; Kennerknecht, Ingo; Müller‐Hofstede, Cornelie; Charbel Issa, Peter; Heller, Raoul; Beck, Bodo; Rüther, Klaus; Mitter, Diana; Rohrschneider, Klaus; Steinhauer, Ute; Korbmacher, Heike M.; Huh...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 5:Issue 5(2017)
Page Start:
531
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗