Analysis of Wallace mutation in patients with Leber's hereditary optic neuropathy: Familial study and tissue distribution

Neuro-Ophthalmology

Volumn 16, Issue 2, 1996, Pages 85-90

  Shimo oku, Masashi ^a  

^a HYOGO COLLEGE OF MEDICINE   (Japan)

Author keywords

Familial study; Leber's hereditary optic atrophy; Mitochondrial DNA; Tissue distribution; Wallace mutation

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; FAMILIAL DISEASE; GENOTYPE; HEREDITARY OPTIC ATROPHY; HUMAN; MALE; MUTATION;

EID: 0029863606     PISSN: 01658107     EISSN: None     Source Type: Journal    
DOI: 10.3109/01658109609009666     Document Type: Article

References (1)

1. Yoneda M, Tsuji S, Yamaguchi T, Inuzuka T, Miyatake T, Horai S, Ozawa T. Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy, Lancet 1989; 1:1076-1077.