DNA diagnosis and clinical features of hereditary optic neuropathy of Leber

Japanese Journal of Clinical Ophthalmology

Volumn 50, Issue 6, 1996, Pages 1179-1182

  Fujimaki, T ^a   Hotta, Y ^a   Hayakawa, M ^a   Yokoyama, T ^a   Takeda, M ^a   Hayatsu, H ^a   Toshida, H ^a   Tamaki, K ^a   Ishida, N ^a   Ishida, M ^a   Ueda, S ^a   Fujiki, K ^a   Kanai, A ^a  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOSTEROID; MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DNA DETERMINATION; FEMALE; HEREDITARY OPTIC ATROPHY; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; STEROID THERAPY; VISUAL ACUITY; VISUAL FIELD DEFECT;

EID: 0029908598     PISSN: 03705579     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)