Congenital primary hypothyroidism with subsequent adenomatous goiter in a Turkish patient caused by a homozygous 10-bp deletion in the thyroid peroxidase (TPO) gene

Clinical Endocrinology

Volumn 64, Issue 5, 2006, Pages 514-518

  Pfarr, Nicole ^a   Musholt, Thomas J ^a   Musholt, Petra B ^a   Brzezinska, Rita ^a   Pohlenz, Joachim ^a  

^a UNIVERSITY MEDICAL CENTER MAINZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; GENOMIC DNA; LEVOTHYROXINE; THYROID PEROXIDASE;

ADOLESCENT; ARTICLE; CASE REPORT; FRAMESHIFT MUTATION; GENE; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC TRANSCRIPTION; GOITER; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HYPOTHYROIDISM; LOW DRUG DOSE; MALE; PRIORITY JOURNAL; RNA TRANSCRIPTION; THYROIDECTOMY; TPO GENE; TURKEY (REPUBLIC);

ADENOMA; ADOLESCENT; CONGENITAL HYPOTHYROIDISM; CONSANGUINITY; GENE DELETION; GOITER, NODULAR; HOMOZYGOTE; HUMANS; IODIDE PEROXIDASE; MALE; PEDIGREE; THYROID FUNCTION TESTS; THYROID HORMONES; THYROIDECTOMY; THYROXINE; TURKEY;

EID: 33645971012     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2006.02500.x     Document Type: Article

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