Mitochondrial DNA depletion in progressive external ophthalmoplegia caused by POLG1 mutations

Acta Neurologica Scandinavica

Volumn 120, Issue SUPPL. 189, 2009, Pages 38-41

  Tzoulis, C ^a,b   Papingji, M ^a   Fiskestrand, T ^a   Roste L S ^c   Bindoff, L A ^a,b  

^a HAUKELAND UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF BERGEN   (Norway)

^c OSLO UNIVERSITY HOSPITAL   (Norway)

Author keywords

Depletion; MtDNA; POLG; Progressive external ophthalmoplegia

Indexed keywords

DNA DIRECTED DNA POLYMERASE GAMMA; MITOCHONDRIAL DNA;

ADULT; AGED; ARTICLE; BINOCULAR CONVERGENCE; BONE BIOPSY; BRAIN; CASE REPORT; CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; CODING; DIPLOPIA; ELECTROMYOGRAPHY; ELECTROPHYSIOLOGY; ENZYME ACTIVE SITE; FEMALE; GENE DELETION; GENE MUTATION; GENE SEQUENCE; HUMAN; HYPOTHYROIDISM; MITOCHONDRIAL DNA DEPLETION; MITOCHONDRIAL GENOME; MUSCLE BIOPSY; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOGENESIS; PERIPHERAL NEUROPATHY; POLG1 GENE; SENSORY NEUROPATHY; SKELETAL MUSCLE; STRUCTURAL GENE;

EID: 67651249896     PISSN: 00016314     EISSN: 16000404     Source Type: Journal    
DOI: 10.1111/j.1600-0404.2009.01212.x     Document Type: Article

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