Exclusion of the human collagen type XVII (COL17A1) gene as the cause of Thiel-Behnke corneal dystrophy (CDB2) on chromosome 10q23-q25

Current Eye Research

Volumn 27, Issue 4, 2003, Pages 223-226

  Sullivan, Lori S ^a   Zhao, Xinping ^b   Bowne, Sara J ^a   Xu, Xiangyang ^b   Daiger, Stephen P ^a   Yee, Steven B ^b   Yee, Richard W ^b,c  

^a UNIVERSITY OF TEXAS SCHOOL OF PUBLIC HEALTH   (United States)

^b UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF TEXAS   (United States)

Author keywords

CDB2; Chromosome 10; Collagen; Corneal dystrophy; Thiel Behnke

Indexed keywords

COLLAGEN TYPE 17; GENOMIC DNA;

ARTICLE; BLOOD SAMPLING; CHROMOSOME 10Q; CHROMOSOME MUTATION; COLLAGEN TYPE 17 GENE; CONTROLLED STUDY; CORNEA DYSTROPHY; DNA FLANKING REGION; DNA ISOLATION; DNA PURIFICATION; DNA SEQUENCE; EVALUATION; EXON; GENE; GENE MAPPING; GENETIC LINKAGE; GENETIC SCREENING; HUMAN; INTRON; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SLIT LAMP; THIEL BEHNKE CORNEAL DYSTROPHY;

ADENINE; AUTOANTIGENS; BASE SEQUENCE; CARRIER PROTEINS; CHROMOSOMES, HUMAN, PAIR 10; COLLAGEN; CORNEAL DYSTROPHIES, HEREDITARY; CYTOSKELETAL PROTEINS; EXONS; HUMANS; INTRONS; NERVE TISSUE PROTEINS; NON-FIBRILLAR COLLAGENS; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; THYMINE; VARIATION (GENETICS);

EID: 0142138819     PISSN: 02713683     EISSN: None     Source Type: Journal    
DOI: 10.1076/ceyr.27.4.223.16595     Document Type: Article

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