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Journal Article
Journal of Neuroscience, ISSN 0270-6474, 03/2016, Volume 36, Issue 11, pp. 3254 - 3267
Journal Article
Journal Article
Mitochondrion, ISSN 1567-7249, 2010, Volume 10, Issue 5, pp. 573 - 578
Journal Article
EMBO reports, ISSN 1469-221X, 08/2018, Volume 19, Issue 8, pp. e45241 - n/a
Charcot–Marie–Tooth disease type 2A (CMT2A) is caused by dominant alleles of the mitochondrial pro‐fusion factor Mitofusin 2 (MFN2). To address the... 
MFN2 | CMT2A | mitochondrial fusion | mitofusin | peripheral neuropathy | MAMMALIAN HOMOLOGS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MARIE-TOOTH DISEASE | AXONAL-TRANSPORT | OPTIC ATROPHY | CELL BIOLOGY | HEREDITARY MOTOR | 2 MUTATIONS | NEURONS | FISSION | PROTEINS | Mitochondrial Dynamics | Neurons - pathology | Neuromuscular Junction - metabolism | Humans | Gain of Function Mutation - genetics | Drosophila Proteins - metabolism | Motor Activity | Mitochondria - ultrastructure | Charcot-Marie-Tooth Disease - genetics | Drosophila melanogaster - metabolism | Neurons - ultrastructure | Membrane Proteins - metabolism | Neurons - metabolism | Disease Models, Animal | Amino Acid Sequence | Membrane Proteins - genetics | Mitochondria - metabolism | Drosophila Proteins - chemistry | Drosophila melanogaster - ultrastructure | Charcot-Marie-Tooth Disease - pathology | Animals | Membrane Proteins - chemistry | Alleles | Mice | Charcot-Marie-Tooth Disease - physiopathology | Drosophila Proteins - genetics | Loss of Function Mutation - genetics | Motor neurons | GTP | Neurons | Pathogenesis | Oxidative metabolism | Drosophila | Agglomeration | Mitochondrial DNA | Neuropathy | Metabolism | Defects | Mitochondria | Insects | Morphology | Charcot-Marie-Tooth disease | Neuromuscular junctions | Mutation | Guanosinetriphosphatase | Life Sciences | Neuroscience | Membrane & Intracellular Transport
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