Thyroperoxidase Gene Mutations in Congenital Goitrous Hypothyroidism with Total and Partial Iodide Organification Defect

Thyroid

Volumn 13, Issue 12, 2003, Pages 1145-1151

  Nascimento, Antonio C ^a   Guedes, Dulce R ^a   Santos, Cecilia S ^a   Knobel, Meyer ^a   Rubio, Ileana G S ^a   Medeiros Neto, Geraldo ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

PERCHLORATE; THYROID PEROXIDASE;

ADOLESCENT; ADULT; APICAL MEMBRANE; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL ARTICLE; CONGENITAL HYPOTHYROIDISM; DISEASE SEVERITY; EXON; GENE INACTIVATION; GENE INSERTION; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; GOITER; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INTRON; NUCLEIC ACID BASE SUBSTITUTION; PARTIAL IODIDE ORGANIFICATION DEFECT; PRIORITY JOURNAL; PROTEIN TRANSPORT; THYROID DISEASE; TOTAL IODIDE ORGANIFICATION DEFECT;

EID: 0347993689     PISSN: 10507256     EISSN: None     Source Type: Journal    
DOI: 10.1089/10507250360731550     Document Type: Article

References (23)

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