Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter gene

Biochemical and Biophysical Research Communications

Volumn 240, Issue 2, 1997, Pages 488-491

  Pohlenz, Joachim ^a   Medeiros Neto, Geraldo ^b   Gross, Jorge L ^c   Silveiro, Sandra P ^c   Knobel, Meyer ^b   Refetoff, Samuel ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

^c HOSPITAL DE CLÍNICAS DE PORTO ALEGRE   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; COTRANSPORTER; IODIDE; MEMBRANE PROTEIN; RECOMBINANT PROTEIN; SODIUM IODIDE SYMPORTER;

ADULT; ANIMAL; ARTICLE; BRAZIL; CASE REPORT; CELL STRAIN COS1; CODON; FEMALE; GENETIC TRANSFECTION; GENETICS; GENOTYPE; HOMOZYGOTE; HUMAN; HYPOTHYROIDISM; MALE; METABOLISM; NUCLEOTIDE SEQUENCE; PEDIGREE; POINT MUTATION; TRANSPORT AT THE CELLULAR LEVEL;

ADULT; ANIMALS; BASE SEQUENCE; BIOLOGICAL TRANSPORT; BRAZIL; CARRIER PROTEINS; CODON; COS CELLS; FEMALE; GENOTYPE; HOMOZYGOTE; HUMANS; HYPOTHYROIDISM; IODIDES; MALE; MEMBRANE PROTEINS; PEDIGREE; POINT MUTATION; RECOMBINANT PROTEINS; SYMPORTERS; TRANSFECTION;

EID: 0031576397     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1997.7594     Document Type: Article

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