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

Erstveröffentlichung

2013

Authors

Eschbach, Judith

Sinniger, Jerome

Bouitbir, Jamal

Fergani, Anissa

Schlagowski, Anna-Isabel

et al.

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.2013.05.015

Institutions

UKU. Klinik für Neurologie

EU 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

Metadata

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