A novel mutation in the thyrotropin (thyroid-stimulating hormone) receptor gene in a case of congenital hypothyroidism

Thyroid

Volumn 16, Issue 12, 2006, Pages 1303-1309

  Jeziorowska, A ^a   Pniewska Siark, B ^a,b   Brzezianska E ^a,b   Pastuszak Lewandoska, D ^a   Lewinski A ^a,b  

^a POLISH MOTHER S MEMORIAL HOSPITAL RESEARCH INSTITUTE   (Poland)

^b MEDICAL UNIVERSITY OF LODZ   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

LEVOTHYROXINE; SODIUM; THYROTROPIN RECEPTOR;

ALLELE; ARTICLE; CHILD; CLINICAL ARTICLE; CONGENITAL HYPOTHYROIDISM; FAMILY HISTORY; GENE MUTATION; GENOTYPE; GOITER; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RECEPTOR GENE; RECESSIVE INHERITANCE; RNA DEGRADATION; THYROID DYSGENESIS; THYROID HORMONE SYNTHESIS; THYROTROPIN RELEASE;

BASE SEQUENCE; CHILD; CODON, NONSENSE; CONGENITAL HYPOTHYROIDISM; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; INFANT, NEWBORN; MALE; PEDIGREE; RECEPTORS, THYROTROPIN;

EID: 33846152599     PISSN: 10507256     EISSN: None     Source Type: Journal    
DOI: 10.1089/thy.2006.16.1303     Document Type: Article

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