OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules
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Title
OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 19, Issue 15, Pages 3043-3052
Publisher
Oxford University Press (OUP)
Online
2010-05-20
DOI
10.1093/hmg/ddq209
References
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Related references
Note: Only part of the references are listed.- Mitochondrial DNA Mutations in Disease, Aging, and Neurodegeneration
- (2010) Amy K. Reeve et al. Annals of the New York Academy of Sciences
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- (2009) Amy K. Reeve et al. AGING CELL
- Emerging roles of mitochondrial proteases in neurodegeneration
- (2009) Paola Martinelli et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Transcriptional and post-transcriptional regulation of mitochondrial biogenesis in skeletal muscle: Effects of exercise and aging
- (2009) Vladimir Ljubicic et al. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
- OPA1 functions in mitochondria and dysfunctions in optic nerve
- (2009) Guy Lenaers et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- OPA1-associated disorders: Phenotypes and pathophysiology
- (2009) Patrizia Amati-Bonneau et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- Nature of Mitochondrial DNA Deletions in Substantia Nigra Neurons
- (2008) Amy K. Reeve et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Hereditary optic neuropathies share a common mitochondrial coupling defect
- (2008) Arnaud Chevrollier et al. ANNALS OF NEUROLOGY
- Progressive External Ophthalmoplegia and Vision and Hearing Loss in a Patient With Mutations in POLG2 and OPA1
- (2008) Silvio Ferraris et al. ARCHIVES OF NEUROLOGY
- OPA1 mutations and mitochondrial DNA damage: keeping the magic circle in shape
- (2008) M. Zeviani BRAIN
- Resistance training in patients with single, large-scale deletions of mitochondrial DNA
- (2008) J. L. Murphy et al. BRAIN
- A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function
- (2008) Marco Spinazzi et al. HUMAN MOLECULAR GENETICS
- Inherited mitochondrial optic neuropathies
- (2008) P Yu-Wai-Man et al. JOURNAL OF MEDICAL GENETICS
- OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
- (2007) P. Amati-Bonneau et al. BRAIN
- 155th ENMC workshop: Polymerase gamma and disorders of mitochondrial DNA synthesis, 21–23 September 2007, Naarden, The Netherlands
- (2007) Patrick F. Chinnery et al. NEUROMUSCULAR DISORDERS
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