Molecular basis of Peters anomaly in Saudi Arabia

Ophthalmic Genetics

Volumn 25, Issue 4, 2004, Pages 257-270

  Edward, Deepak P ^a,b   Al Rajhi, Ali ^b   Lewis, Richard Alan ^c   Curry, Stacey A ^c   Wang, Zongren ^d   Bejjani, Bassem A ^c,d  

^a UNIVERSITY OF ILLINOIS   (United States)

^b KING KHALED EYE SPECIALIST HOSPITAL   (Saudi Arabia)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d WASHINGTON STATE UNIVERSITY   (United States)

Author keywords

CYP1B1; Cytochrome; Molecular basis; P4501B1; Peters anomaly; Saudi Arabia

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; CORNEA; DISEASE SEVERITY; EXON; FEMALE; GENE EXPRESSION; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; HEALTH PRACTITIONER; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; MALE; MOLECULAR DYNAMICS; OPHTHALMOLOGY; PATHOPHYSIOLOGY; PETERS ANOMALY; PHENOTYPE; PRIORITY JOURNAL; RELATIVE; RIEGER SYNDROME; SAUDI ARABIA;

ARYL HYDROCARBON HYDROXYLASES; BIOLOGICAL MARKERS; CORNEAL OPACITY; DNA-BINDING PROTEINS; EYE PROTEINS; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GLAUCOMA; HOMEODOMAIN PROTEINS; HOMOZYGOTE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; PAIRED BOX TRANSCRIPTION FACTORS; PEDIGREE; REPRESSOR PROTEINS; SAUDI ARABIA; TRANSCRIPTION FACTORS;

EID: 12344300314     PISSN: 13816810     EISSN: None     Source Type: Journal    
DOI: 10.1080/13816810490902648     Document Type: Article

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