Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis

Annals of Neurology

Volumn 36, Issue 1, 1994, Pages 109-112

  Kellar Wood H ^a   Robertson, N ^a   Govan, G G ^b   Compston, D A S ^a   Harding, A E ^b  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA BASE; MITOCHONDRIAL DNA;

ADULT; ARTICLE; CONTROLLED STUDY; GENE MUTATION; GENETIC COUNSELING; GENETIC HETEROGENEITY; GENETIC SUSCEPTIBILITY; HEREDITARY OPTIC ATROPHY; HUMAN; MAJOR CLINICAL STUDY; MULTIPLE SCLEROSIS; PATHOGENESIS; PRIORITY JOURNAL; VISUAL ACUITY; VISUAL IMPAIRMENT;

ADULT; BASE SEQUENCE; BRAIN; COMORBIDITY; DISEASES IN TWINS; DNA, MITOCHONDRIAL; FAMILY; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MOLECULAR SEQUENCE DATA; MULTIPLE SCLEROSIS; MUTATION; OPTIC ATROPHIES, HEREDITARY; SEX FACTORS;

EID: 0028337837     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.410360121     Document Type: Article

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