Progressive External Ophthalmoplegia Characterized by Multiple Deletions of Mitochondrial DNA: Unraveling the Pathogenesis of Human Mitochondrial DNA Instability and the Initiation of a Genetic Classification

By Van Goethem Gert   Martin Jean-Jacques   Van Broeckhoven Christine  

NeuroMolecular Medicine, Vol. 3, Iss. 3, 2003-06 ,pp. : 129-146

Humana Press, Inc

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OPA1 mutations induce mitochondrial DNA instability and optic atrophy â–˜plusâ–™ phenotypes

By Amati-Bonneau Patrizia  

Brain, Vol. 131, Iss. 2, 2008-02 ,pp. : 338-351

Oxford University Press

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OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion

By Zanna Claudia  

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Oxford University Press

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A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia

By Deschauer M.   Kiefer R.   Blakely E.L.   He L.   Zierz S.   Turnbull D.M.   Taylor R.W.  

Neuromuscular Disorders, Vol. 13, Iss. 7, 2003-09 ,pp. : 568-572

Elsevier

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Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions

By Taivassalo Tanja   Gardner Julie L.   Schaefer Andrew M.   Newman Jane   Barron Martin J.   Haller Ronald G.   Turnbull Douglass M.  

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Oxford University Press

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