Periodically hyperthyroid phenotype in thyroid hormone resistance is associated with mutation D322N in the thyroid hormone receptor β gene: Transcriptional properties of the mutant and the role of retinoid X receptor

Experimental and Clinical Endocrinology and Diabetes

Volumn 104, Issue , 1996, Pages 111-116

  Behr, Michael ^a   Loos, Ulrich ^a  

^a UNIVERSITY OF ULM   (Germany)

Author keywords

Mutation; resistance; retinoid X receptor; thyroid hormone receptor

Indexed keywords

RETINOID X RECEPTOR; THYROID HORMONE RECEPTOR;

ADULT; AMINO ACID SUBSTITUTION; CASE REPORT; CONFERENCE PAPER; FEMALE; HUMAN; HYPERTHYROIDISM; MALE; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; THYROID HORMONE RESISTANCE;

ADULT; CHILD, PRESCHOOL; CODON; HUMANS; HYPERTHYROIDISM; MALE; PHENOTYPE; POINT MUTATION; RECEPTORS, RETINOIC ACID; RECEPTORS, THYROID HORMONE; RETINOID X RECEPTORS; THYROID HORMONE RESISTANCE SYNDROME; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC; TRIIODOTHYRONINE;

EID: 0029906771     PISSN: 09477349     EISSN: 14393646     Source Type: Journal    
DOI: 10.1055/s-0029-1211716     Document Type: Article

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