Genetic skin diseases with altered aging

Archives of Dermatology

Volumn 133, Issue 10, 1997, Pages 1293-1295

  Goldsmith, Lowell A ^a  

^a BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; AUTOANTIBODY; CALCIUM BINDING PROTEIN; COMPLEMENTARY DNA; DOUBLE STRANDED DNA; FIBRONECTIN; GENE PRODUCT; HELICASE; MESSENGER RNA; OSTEONECTIN; PLASMINOGEN ACTIVATOR INHIBITOR 1; PROTEIN; PROTEIN P53; SOMATOMEDIN BINDING PROTEIN 3; SPHINGOMYELIN PHOSPHODIESTERASE;

AGING; CLINICAL FEATURE; COCKAYNE SYNDROME; GENE; GENE MUTATION; GENETIC DISORDER; HUMAN; ONCOGENE C FOS; PHENOTYPE; PLEIOTROPY; PRIORITY JOURNAL; REVIEW; SKIN DISEASE; WERNER SYNDROME;

EID: 0030841386     PISSN: 0003987X     EISSN: None     Source Type: Journal    
DOI: 10.1001/archderm.133.10.1293     Document Type: Review

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