A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency

Science

Volumn 257, Issue 5073, 1992, Pages 1115-1118

  Radovick, Sally ^a,d   Nations, Michelle ^b   Du, Yuefen ^a   Berg, LaVonne A ^b   Weintraub, Bruce D ^c   Wondisford, Fredric E ^b,e  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^c NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^d BOSTON CHILDREN S HOSPITAL   (United States)

^e BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MAMMALIA;

HYPOPHYSIS HORMONE; TRANSCRIPTION FACTOR;

ARTICLE; CASE REPORT; DEVELOPMENT; DWARFISM; HORMONE DEFICIENCY; HUMAN; HYPOPHYSIS; MOUSE; MUTATION; NONHUMAN; PRIORITY JOURNAL;

ALLELES; AMINO ACID SEQUENCE; BASE SEQUENCE; BINDING SITES; CASE REPORT; DNA; DNA-BINDING PROTEINS; GROWTH HORMONE; HUMAN; MOLECULAR SEQUENCE DATA; MUTATION; PITUITARY GLAND, ANTERIOR; PITUITARY HORMONES; POLYMERASE CHAIN REACTION; PROLACTIN; PROMOTER REGIONS (GENETICS); SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; THYROTROPIN; TRANSCRIPTION FACTORS; TRANSFECTION;

EID: 0026767630     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.257.5073.1115     Document Type: Article

References (0)