Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxias

DSpace Repository

Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxias

Author: Bis, Dana M.; Schuele, Rebecca; Reichbauer, Jennifer; Synofzik, Matthis; Rattay, Tim W.; Soehn, Anne; de Jonghe, Peter; Schoels, Ludger; Zuchner, Stephan
Tübinger Autor(en):
Reichbauer, Jennifer
Schüle, Rebecca
Synofzik, Matthis Benjamin
Rattay, Tim Wilfried
Söhn, Anne
Schöls, Ludger
Published in: Molecular Genetics & Genomic Medicine (2017), Bd. 5, H. 3, S. 280-286
Verlagsangabe: Wiley
Language: English
Full text: http://dx.doi.org/10.1002/mgg3.285
ISSN: 2324-9269
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
Show full item record

This item appears in the following Collection(s)