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

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

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

Autor(en):

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
Bender, Benjamin
Schüle-Freyer, Rebecca

Erschienen in:

Journal of Neurology (2015), Bd. 262, H. 9, S. 2124-2134

Verlagsangabe:

Springer Heidelberg

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1007/s00415-015-7727-2

ISSN:

0340-5354