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Volumn 1, Issue 10, 1996, Pages 460-464
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Constitutively activating mutations of the thyrotropin receptor and thyroid disease.
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Author keywords
[No Author keywords available]
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Indexed keywords
THYROTROPIN RECEPTOR;
AMINO ACID SEQUENCE;
CHEMICAL STRUCTURE;
CHEMISTRY;
GENETICS;
HUMAN;
HYPERTHYROIDISM;
MOLECULAR GENETICS;
PATHOPHYSIOLOGY;
PHYSIOLOGY;
POINT MUTATION;
PROTEIN CONFORMATION;
REVIEW;
THYROID DISEASE;
THYROID GLAND;
THYROID TUMOR;
AMINO ACID SEQUENCE;
HUMANS;
HYPERTHYROIDISM;
MODELS, MOLECULAR;
MOLECULAR SEQUENCE DATA;
POINT MUTATION;
PROTEIN CONFORMATION;
RECEPTORS, THYROTROPIN;
THYROID DISEASES;
THYROID GLAND;
THYROID NEOPLASMS;
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EID: 0030601152
PISSN: 09492321
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
Times cited : (6)
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References (39)
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