Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1

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Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1

Author: Strickland, Alleene V.; Schabhuettl, Maria; Offenbacher, Hans; Synofzik, Matthis; Hauser, Natalie S.; Brunner-Krainz, Michaela; Gruber-Sedlmayr, Ursula; Moore, Steven A.; Windhager, Reinhard; Bender, Benjamin; Harms, Matthew; Klebe, Stephan; Young, Peter; Kennerson, Marina; Garcia, Avencia Sanchez Mejias; Gonzalez, Michael A.; Zuechner, Stephan; Schule, Rebecca; Shy, Michael E.; Auer-Grumbach, Michaela
Tübinger Autor(en):
Synofzik, Matthis Benjamin
Bender, Benjamin
Schüle-Freyer, Rebecca
Published in: Journal of Neurology (2015), Bd. 262, H. 9, S. 2124-2134
Verlagsangabe: Springer Heidelberg
Language: English
Full text: http://dx.doi.org/10.1007/s00415-015-7727-2
ISSN: 0340-5354
DDC Classifikation: 610 - Medicine and health
Dokumentart: Artikel
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