Leber's hereditary optic neuropathy in Thailand

Japanese Journal of Ophthalmology

Volumn 45, Issue 6, 2001, Pages 665-668

  Chuenkongkaew, Wanicha L ^a   Lertrit, Patcharee ^a   Poonyathalang, Anuchit ^a   Sura, Thanyachai ^a   Atchaneeyasakul, L ^a   Suphavilai, Rungnapa ^a  

^a MAHIDOL UNIVERSITY   (Thailand)

Author keywords

11778 mutation; Leber's hereditary optic neuropathy; Thailand

Indexed keywords

MITOCHONDRIAL DNA; NUCLEOTIDE; RESTRICTION ENDONUCLEASE;

ADOLESCENT; ADULT; ARTICLE; ASIAN; BLINDNESS; CHILD; CONTROLLED STUDY; DISEASE TRANSMISSION; ENZYME ANALYSIS; EUROPE; FEMALE; FOLLOW UP; HEREDITARY OPTIC ATROPHY; HUMAN; HYPEREMIA; INJURY; MAJOR CLINICAL STUDY; MALE; MUTATION; ONSET AGE; PEDIGREE; POPULATION RESEARCH; PRIORITY JOURNAL; TELANGIECTASIA; THAILAND; UNITED STATES; VISUAL ACUITY; VISUAL IMPAIRMENT;

ADOLESCENT; ADULT; AGE OF ONSET; CHILD; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; EUROPE; FEMALE; HUMANS; JAPAN; MALE; MIDDLE AGED; MUTATION; OPTIC ATROPHY, HEREDITARY, LEBER; PEDIGREE; THAILAND; UNITED STATES;

EID: 0035689731     PISSN: 00215155     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0021-5155(01)00423-3     Document Type: Article

References (4)

1. Clinical features of Japanese Leber's hereditary optic neuropathy with the 11778 mutation of mitochondrial DNA
2. Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy
3. The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation
4. The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation