Mitochondrial DNA nucleotide changes in primary congenital glaucoma patients

Molecular Vision

Volumn 19, Issue , 2013, Pages 220-230

  Kumar, Manoj ^a   Tanwar, Mukesh ^a   Faiq, Muneeb Ahmad ^b   Pani, Jhumur ^a   Shamsi, Monis Bilal ^a   Dada, Tanuj ^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

ALANINE; CYTOCHROME B; CYTOCHROME C OXIDASE; CYTOCHROME P450 1B1; CYTOSINE; GLYCINE; MITOCHONDRIAL DNA; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); RIBOSOME RNA; TRANSFER RNA; UBIQUINOL CYTOCHROME C REDUCTASE;

ARTICLE; BLOOD SAMPLING; CHILD; CLINICAL ARTICLE; CONGENITAL GLAUCOMA; CONTROLLED STUDY; CYP1B1 GENE; DNA SEQUENCE; FEMALE; FOXC1 GENE; FRAMESHIFT MUTATION; GENE; GENETIC VARIABILITY; HUMAN; INFANT; LTBP2 GENE; MALE; MITOCHONDRIAL GENOME; MOLECULAR MODEL; MOLECULAR PHYLOGENY; MYOC GENE; NUCLEOTIDE SEQUENCE; PHENOTYPIC VARIATION; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIMARY GLAUCOMA; PRIORITY JOURNAL; RESPIRATORY CHAIN; RNA GENE; SEQUENCE ANALYSIS; STOP CODON; TRANSCRIPTION TERMINATION;

CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; CYTOCHROMES B; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX IV; FEMALE; GENETIC VARIATION; GENOME, MITOCHONDRIAL; GLAUCOMA; HAPLOTYPES; HUMANS; INFANT; MALE; MITOCHONDRIAL PROTON-TRANSLOCATING ATPASES; MUTATION; NADH DEHYDROGENASE;

EID: 84873565312     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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