Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts

Human Molecular Genetics

Volumn 10, Issue 3, 2001, Pages 231-236

  Semina, Elena V ^a   Brownell, Isaac ^c   Mintz Hittner, Helen A ^d   Murray, Jeffrey C ^a,b   Jamrich, Milan ^c  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; FOXE3 PROTEIN; GUANINE; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANTERIOR EYE SEGMENT; ARTICLE; CATARACT; CHILDHOOD DISEASE; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DNA FLANKING REGION; EYE DISEASE; EYE MALFORMATION; FAMILY; FRAMESHIFT MUTATION; GENE INSERTION; GENE MUTATION; GENETIC CODE; GENETIC HETEROGENEITY; GLAUCOMA; HUMAN; HUMAN CELL; LENS EPITHELIUM; MAJOR CLINICAL STUDY; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PREDICTION; PRIORITY JOURNAL; STOP CODON; VISUAL IMPAIRMENT;

EID: 0035253581     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.3.231     Document Type: Article

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