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Volumn 275, Issue 51, 2000, Pages 39831-39836

Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 leber's hereditary optic neuropathy mitochondrial DNA mutation

(5) Brown, Michael D a Trounce, Ian A b Jun, Albert S a Allen, Jon C a Wallace, Douglas C a

a EMORY UNIVERSITY SCHOOL OF MEDICINE (United States)

b ST VINCENT S HOSPITAL (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; MITOCHONDRIAL ENZYME;

ARTICLE; CONTROLLED STUDY; ENZYME ANALYSIS; ENZYME ASSAY; ENZYME DEFECT; GENE MUTATION; HUMAN; HUMAN CELL; HYBRID CELL; LEBER CONGENITAL AMAUROSIS; LYMPHOBLAST; MITOCHONDRIAL RESPIRATION; OPTIC NERVE DISEASE; OXIDATIVE PHOSPHORYLATION; PATHOPHYSIOLOGY; POLAROGRAPHY; PRIORITY JOURNAL;

CELL LINE; DNA, MITOCHONDRIAL; FEMALE; HUMANS; LYMPHOCYTES; MALE; MUTATION; OPTIC ATROPHIES, HEREDITARY; POLAROGRAPHY;

EID: 0034704125 PISSN: 00219258 EISSN: None Source Type: Journal
DOI: 10.1074/jbc.M006476200 Document Type: Article

Times cited : (236)

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