COLdb, a database linking genetic data to molecular function in fibrillar collagens

Human Mutation

Volumn 30, Issue 6, 2009, Pages 946-951

  Bodian, Dale L ^a   Klein, Teri E ^a,b  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b STANFORD UNIVERSITY   (United States)

Author keywords

COL1A1; COL1A2; COL2A1; COL3A1; Collagen; Connective tissue disorders; Fibrillar collagens; Genotype phenotype relationships; Locus specific database; Mutations; Skeletal dysplasias; SNPs

Indexed keywords

COLLAGEN TYPE 1; COLLAGEN TYPE 2; COLLAGEN TYPE 3; FIBRILLAR COLLAGEN;

AMINO ACID SEQUENCE; CHONDRODYSPLASIA; COL2A1 GENE; EHLERS DANLOS SYNDROME; GENE; GENE FUNCTION; GENE MUTATION; GENETIC DATABASE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; NUCLEOTIDE SEQUENCE; OSTEOGENESIS IMPERFECTA; PHENOTYPE; PHYSICAL CHEMISTRY; PRIORITY JOURNAL; PROTEIN SYNTHESIS; REVIEW;

ACCESS TO INFORMATION; COLLAGEN TYPE II; COMPUTER GRAPHICS; DATABASES, GENETIC; FIBRILLAR COLLAGENS; HUMANS; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, PROTEIN;

EID: 66349112586     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20978     Document Type: Review

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