C-terminal amino acid alteration rather than late termination causes complete deficiency of thyroxine-binding globulin CD-neuIsenburg

Journal of Clinical Endocrinology and Metabolism

Volumn 91, Issue 8, 2006, Pages 3215-3218

  Moeller, Lars C ^a   Fingerhut, Anja ^a   Lahner, Harald ^a   Grasberger, Helmut ^b   Weimer, Bernd ^c   Happ, Joachim ^c   Mann, Klaus ^a   Janssen, Onno E ^a  

^a UNIVERSITY HOSPITAL ESSEN   (Germany)

^b UNIVERSITY OF CHICAGO   (United States)

^c Endokrinologische Gemeinschaftspraxis   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; THYROXINE BINDING GLOBULIN;

ADULT; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; CARBOXY TERMINAL SEQUENCE; CASE REPORT; DNA SEQUENCE; FRAMESHIFT MUTATION; GENE AMPLIFICATION; GENE DELETION; GENE EXPRESSION; GENE MUTATION; GERMANY; GLYCOSYLATION; HUMAN; HUMAN CELL; IN VITRO STUDY; MALE; MUTAGENESIS; OOCYTE; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DEFICIENCY; PROTEIN SECRETION; PROTEIN VARIANT; THYROID FUNCTION TEST; WESTERN BLOTTING; XENOPUS;

EID: 33747644918     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2005-2261     Document Type: Article

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