Congenital goitrous hypothyroidism: Mutation analysis in the thyroid peroxidase gene

Clinical Endocrinology

Volumn 76, Issue 4, 2012, Pages 568-576

  Belforte, Fiorella S ^a   Miras, Mirta B ^b   Olcese, María C ^a   Sobrero, Gabriela ^b   Testa, Graciela ^b   Muñoz, Liliana ^b   Gruñeiro Papendieck, Laura ^c   Chiesa, Ana ^c   González Sarmiento, Rogelio ^d   Targovnik, Héctor M ^a,d   Rivolta, Carina M ^a,d  

^a UNIVERSIDAD DE BUENOS AIRES   (Argentina)

^b Hospital de Ninos de la Santisima Trinidad   (Argentina)

^c HOSPITAL DE NIÑOS RICARDO GUTIÉRREZ   (Argentina)

^d UNIVERSITY OF SALAMANCA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; LEVOTHYROXINE; LIOTHYRONINE; THYROID PEROXIDASE; THYROTROPIN; THYROXINE;

ADOLESCENT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CLINICAL ARTICLE; COMPUTER MODEL; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; DNA SEQUENCE; FEMALE; FREE THYROXINE INDEX; GENE INSERTION; GENE MUTATION; GENETIC HETEROGENEITY; HETEROZYGOTE; HOMOZYGOTE; HUMAN; IODIDE ORGANIFICATION DEFECT; LABORATORY TEST; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NEWBORN SCREENING; NODULAR GOITER; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; SCHOOL CHILD; SEQUENCE HOMOLOGY; SINGLE STRAND CONFORMATION POLYMORPHISM; THYROID DISEASE; THYROID SCINTISCANNING;

ADOLESCENT; CHILD; CONGENITAL HYPOTHYROIDISM; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; IODIDE PEROXIDASE; MALE; MUTATION;

EID: 84857858404     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2011.04249.x     Document Type: Article

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