A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons

Erstveröffentlichung

2010

Authors

Braunstein, Kerstin E.

Eschbach, Judith

Rona-Voeroes, Krisztina

Soylu, Rana

Mikrouli, Elli

et al.

Wissenschaftlicher Artikel

Published in

Human Molecular Genetics ; 19 (2010), 22. - S. 4385-4398. - ISSN 0964-6906. - eISSN 1460-2083

Link to publication

https://dx.doi.org/10.1093/hmg/ddq361

Institutions

UKU. Klinik für Neurologie

Subject headings

[Free subject headings]: HUNTINGTIN-ASSOCIATED PROTEIN | AXONAL-TRANSPORT DEFECTS | DISEASE TRANSGENIC MICE | MOTOR-NEURONS | NEUROTROPHIC FACTOR | MOUSE MODEL | DYNEIN/DYNACTIN FUNCTION | VESICULAR TRANSPORT | SENSORY NEUROPATHY | MUTANT DYNACTIN
[DDC subject group]: DDC 570 / Life sciences

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