Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation
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Title
Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation
Authors
Keywords
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Journal
eLife
Volume 5, Issue -, Pages -
Publisher
eLife Sciences Organisation, Ltd.
Online
2016-08-06
DOI
10.7554/elife.16078
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Note: Only part of the references are listed.- Loss of OMA1 delays neurodegeneration by preventing stress-induced OPA1 processing in mitochondria
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- Disturbed mitochondrial dynamics and neurodegenerative disorders
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- Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells
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- The dynamin-related GTPase Drp1 is required for embryonic and brain development in mice
- (2009) Junko Wakabayashi et al. JOURNAL OF CELL BIOLOGY
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