Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy

Molecular Vision

Volumn 16, Issue , 2010, Pages 782-792

  Kumar, Manoj ^a   Tanwar, Mukesh ^a   Saxena, Rohit ^b   Sharma, Pradeep ^b   Dada, Rima ^a  

^a ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

^b ALL INDIA INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE;

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SCREENING; DNA SEQUENCE; ENZYME SYNTHESIS; GENE AMPLIFICATION; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HOMEOSTASIS; HUMAN; LEBER HEREDITARY OPTIC NEUROPATHY; MALE; NUCLEOTIDE SEQUENCE; OPHTHALMOSCOPY; OXIDATIVE STRESS; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; RETINA GANGLION CELL; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS; SLIT LAMP;

ADULT; DNA, MITOCHONDRIAL; GENETIC TESTING; HUMANS; MALE; MUTATION; OPTIC ATROPHY, HEREDITARY, LEBER; PHENOTYPE; POLYMORPHISM, GENETIC; YOUNG ADULT;

EID: 77955621516     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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