Optic neuropathy in Lhon and Leigh syndrome [4]

Ophthalmology

Volumn 108, Issue 7, 2001, Pages 1172-1173

  Carelli, Valerio ^a   Sadun, Alfredo A ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; DISEASE COURSE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; HEREDITARY OPTIC ATROPHY; HISTOPATHOLOGY; HUMAN; LEIGH DISEASE; LETTER; OPTIC NERVE DISEASE; POINT MUTATION; PRIORITY JOURNAL;

EID: 0034976981     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(01)00618-2     Document Type: Letter

References (8)

1. Ocular histopathologic study of a patient with the T8993-G point mutation in Leigh's syndrome
2. Mitochondrial DNA mutation and pathogenesis
3. Pathogenic factors underlying the lesions in Leigh's disease. Tissue responses to cellular energy deprivation and their clinico-pathological consequences
4. Acquired mitochondrial impairment as a cause of optic nerve disease
5. Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families
6. Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation
7. Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy
8. A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase