Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene

Clinical Endocrinology

Volumn 70, Issue 4, 2009, Pages 623-628

  Supornsilchai, Vichit ^a   Sahakitrungruang, Taninee ^a   Wongjitrat, Nattakarn ^a   Wacharasindhu, Suttipong ^a   Suphapeetiporn, Kanya ^a,b   Shotelersuk, Vorasuk ^a  

^a CHULALONGKORN UNIVERSITY   (Thailand)

^b KING CHULALONGKORN MEMORIAL HOSPITAL   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; LIOTHYRONINE; METHIONINE; PROPRANOLOL; PROPYLTHIOURACIL; RADIOACTIVE IODINE; THREONINE; THYROTROPIN; THYROTROPIN RECEPTOR; THYROXINE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; BLOOD SAMPLING; BONE MALFORMATION; BRAIN VENTRICLE DILATATION; CASE REPORT; CHILD; CLINICAL FEATURE; DISEASE SEVERITY; DNA SEQUENCE; EXON; FEMALE; FINGER; GENE MUTATION; GENE SEQUENCE; HAND RADIOGRAPHY; HUMAN; HYPERTHYROIDISM; INFANT; LEUKOCYTE; LIOTHYRONINE BLOOD LEVEL; MALE; METACARPAL BONE; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PHALANX; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SUBTOTAL THYROIDECTOMY; THYROTROPIN BLOOD LEVEL; THYROXINE BLOOD LEVEL;

ADULT; CHILD, PRESCHOOL; DNA; FEMALE; FINGER PHALANGES; GERM-LINE MUTATION; HEART DEFECTS, CONGENITAL; HEART VENTRICLES; HUMANS; HYPERTHYROIDISM; INFANT; MALE; PEDIGREE; PHENOTYPE; RECEPTORS, THYROTROPIN; THAILAND;

EID: 61449236444     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2008.03367.x     Document Type: Article

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