Complex I respiratory defect in LHON plus dystonia with no mitochondrial DNA mutation [13]

British Journal of Ophthalmology

Volumn 89, Issue 10, 2005, Pages 1380-1381

  Abu Amero, Khaled K ^a   Bosley, T M ^a   Bohlega, S ^a   McLean, D ^a  

^a KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

ADOLESCENT; ANAMNESIS; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; DISEASE COURSE; DISEASE SEVERITY; DYSTONIA; FEMALE; HUMAN; LABORATORY TEST; LEBER HEREDITARY OPTIC NEUROPATHY; LETTER; MUTATION; PATHOLOGY; PRIORITY JOURNAL; RESPIRATORY TRACT DISEASE; GENETICS;

ADOLESCENT; DNA, MITOCHONDRIAL; DYSTONIC DISORDERS; ELECTRON TRANSPORT COMPLEX I; FEMALE; HUMANS; MUTATION; OPTIC ATROPHY, HEREDITARY, LEBER;

EID: 27744438627     PISSN: 00071161     EISSN: None     Source Type: Journal    
DOI: 10.1136/bjo.2005.072819     Document Type: Letter

References (7)

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