Two novel mutations in the thyroid peroxidase gene with goitrous hypothyroidism

Endocrine Journal

Volumn 52, Issue 5, 2005, Pages 643-645

  Tajima, Toshihiro ^a   Tsubaki, Junko ^a   Fujieda, Kenji ^b  

^a HOKKAIDO UNIVERSITY   (Japan)

^b ASAHIKAWA MEDICAL COLLEGE   (Japan)

Author keywords

Goitrous hypothyroidism; Iodide organification defect; Thyroid peroxidase gene; TPO

Indexed keywords

IODIDE; LEVOTHYROXINE; THYROID PEROXIDASE;

ADULT; ARTICLE; CASE REPORT; EXON; GENE AMPLIFICATION; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GOITER; HETEROZYGOSITY LOSS; HUMAN; HYPOTHYROIDISM; INTRON; IODINATION; MALE; SEQUENCE ANALYSIS; THYROID GLAND;

ADOLESCENT; CHILD, PRESCHOOL; CONGENITAL HYPOTHYROIDISM; GENE DELETION; GOITER; HUMANS; INFANT, NEWBORN; IODIDE PEROXIDASE; MALE; MUTATION, MISSENSE;

EID: 27744477800     PISSN: 09188959     EISSN: 13484540     Source Type: Journal    
DOI: 10.1507/endocrj.52.643     Document Type: Article

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