Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age

Erstveröffentlichung
2013Authors
Eschbach, Judith
Sinniger, Jerome
Bouitbir, Jamal
Fergani, Anissa
Schlagowski, Anna-Isabel
Wissenschaftlicher Artikel
Published in
Neurobiology of Disease ; 58 (2013). - S. 220-230. - ISSN 0969-9961
Link to publication
https://dx.doi.org/10.1016/j.nbd.2013.05.015Institutions
UKU. Klinik für NeurologieEU Project uulm
EURO-MOTOR / European multidisciplinary ALS network identification to cure motor neuron degeneration / EC / FP7 / 259867
Subject headings
[Free subject headings]: Dynein | Spinal muscular atrophy | Motor neuron disease | Charcot-Marie-Tooth disease | Mitochondria | Diabetes | MARIE-TOOTH-DISEASE | NEURONAL MIGRATION DEFECTS | TYPE-2 DIABETES-MELLITUS | CYTOPLASMIC DYNEIN | SENSORY NEUROPATHY | DNA INSTABILITY | MOUSE MODEL | AXON LOSS | TRANSPORT | GENE[DDC subject group]: DDC 570 / Life sciences | DDC 610 / Medicine & health