A common structural mechanism underlying GCMB mutations that cause hypoparathyroidism

Medical Hypotheses

Volumn 67, Issue 3, 2006, Pages 482-487

  Sticht, Heinrich ^a   Hashemolhosseini, Said ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR GCMB; UNCLASSIFIED DRUG;

ARTICLE; DNA BINDING; DNA BINDING MOTIF; DNA PROTEIN COMPLEX; GENETIC ASSOCIATION; HYPOPARATHYROIDISM; MOLECULAR DYNAMICS; MOLECULAR INTERACTION; MUTAGENESIS; MUTANT; MUTATION; PARATHYROID GLAND; PRIORITY JOURNAL; TRANSACTIVATION; WILD TYPE;

AMINO ACID SEQUENCE; CONSERVED SEQUENCE; DNA-BINDING PROTEINS; HUMANS; HYDROGEN BONDING; HYPOPARATHYROIDISM; MODELS, GENETIC; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; NUCLEAR PROTEINS; POINT MUTATION; PREDICTIVE VALUE OF TESTS; PROTEIN CONFORMATION; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; SENSITIVITY AND SPECIFICITY; SEQUENCE HOMOLOGY, AMINO ACID; TRANS-ACTIVATION (GENETICS); TRANSCRIPTION FACTORS; VARIATION (GENETICS);

EID: 33745246584     PISSN: 03069877     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mehy.2006.01.062     Document Type: Article

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