Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome

Human Molecular Genetics

Volumn 7, Issue 7, 1998, Pages 1113-1117

  Kulak, Stephen C ^a   Kozlowski, Kathy ^a   Semina, Elena V ^b   Pearce, William G ^a   Walter, Michael A ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

^b UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; HISTIDINE;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; AXENFELD RIEGER SYNDROME; CHROMOSOME 4Q; CRANIOFACIAL MALFORMATION; EYE MALFORMATION; GENE MUTATION; HUMAN; IRIDOGONIODYSGENESIS; MOLECULAR CLONING; PHENOTYPE; PRIORITY JOURNAL; RIEGER SYNDROME;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; ANTERIOR CHAMBER; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, DOMINANT; HOMEODOMAIN PROTEINS; HUMANS; IRIS; MALE; MOLECULAR SEQUENCE DATA; NUCLEAR PROTEINS; PAIRED BOX TRANSCRIPTION FACTORS; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SYNDROME; TRANSCRIPTION FACTORS;

EID: 0031802075     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.7.1113     Document Type: Article

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