Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion
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Title
Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion
Authors
Keywords
Mitofusin 2, Mitochondrial DNA, Depletion, Deletion, Charcot–Marie–Tooth neuropathy type 2A
Journal
ACTA NEUROPATHOLOGICA
Volume 125, Issue 2, Pages 245-256
Publisher
Springer Nature
Online
2012-08-27
DOI
10.1007/s00401-012-1036-y
References
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- Repeats, longevity and the sources of mtDNA deletions: evidence from ‘deletional spectra’
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- Phenotypic spectrum of MFN2 mutations in the Spanish population
- (2009) C. Casasnovas et al. JOURNAL OF MEDICAL GENETICS
- Mitofusins and OPA1 Mediate Sequential Steps in Mitochondrial Membrane Fusion
- (2009) Zhiyin Song et al. MOLECULAR BIOLOGY OF THE CELL
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- (2008) Elizabeth A. Amiott et al. EXPERIMENTAL NEUROLOGY
- Influence of mitochondrial DNA level on cellular energy metabolism: implications for mitochondrial diseases
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- Clonally Expanded Mitochondrial DNA Mutations in Epileptic Individuals With Mutated DNA Polymerase γ
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- Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells
- (2008) Andrey V Kuznetsov et al. Nature Protocols
- OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
- (2007) P. Amati-Bonneau et al. BRAIN
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