Evaluation of serum levels of SOD and MDA in patients with Leber's hereditary optic neuropathy carrying the mitochondrial DNA G11778A mutation

Chinese Journal of Ophthalmology

Volumn 45, Issue 8, 2009, Pages 719-723

  Liu, Zhe ^a   Sun, Chuan Bin ^a   Tong, Yi ^a   Qu, Jia ^a  

^a ZHEJIANG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

Hereditary; Leber; Malondialdehyde; Optic Atrophy; Superoxide dismutase

Indexed keywords

MALONALDEHYDE; MITOCHONDRIAL DNA; SUPEROXIDE DISMUTASE;

ADOLESCENT; ADULT; ARTICLE; BLOOD; CASE CONTROL STUDY; FEMALE; GENETICS; HUMAN; LEBER HEREDITARY OPTIC NEUROPATHY; MALE; MIDDLE AGED; MUTATION;

ADOLESCENT; ADULT; CASE-CONTROL STUDIES; DNA, MITOCHONDRIAL; FEMALE; HUMANS; MALE; MALONDIALDEHYDE; MIDDLE AGED; MUTATION; OPTIC ATROPHY, HEREDITARY, LEBER; SUPEROXIDE DISMUTASE; YOUNG ADULT;

EID: 69549135971     PISSN: 04124081     EISSN: None     Source Type: Journal    
DOI: 10.3760/cma.j.issn.0412-4081.2009.08.011     Document Type: Article

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