A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect

Clinical Endocrinology

Volumn 51, Issue 2, 1999, Pages 165-172

  Santos, Cecilia L S ^a   Bikker, Hennie ^c   Rego, Katia G M ^a   Nascimento, Antonio C ^a   Tambascia, Marcos ^b   De Vijlder, Jan J M ^c   Medeiros Neto, Geraldo ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b UNIVERSITY OF CAMPINAS   (Brazil)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

IODIDE; LEVOTHYROXINE; LIOTHYRONINE; PERCHLORATE; THYROGLOBULIN; THYROID HORMONE; THYROXINE;

ADULT; ARTICLE; CLINICAL ARTICLE; DENATURING GRADIENT GEL ELECTROPHORESIS; EXON; FRAMESHIFT MUTATION; GENE MUTATION; GOITER; HUMAN; HYPOTHESIS; HYPOTHYROIDISM; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; THYROID HORMONE BLOOD LEVEL;

ADOLESCENT; ADULT; CHILD; CONGENITAL HYPOTHYROIDISM; ELECTROPHORESIS, POLYACRYLAMIDE GEL; FEMALE; FRAMESHIFT MUTATION; GOITER; HUMANS; HYPOTHYROIDISM; IODIDE PEROXIDASE; MALE; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA;

EID: 0032768958     PISSN: 03000664     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2265.1999.00746.x     Document Type: Article

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