A novel peculiar mutation in the sodium/iodide symporter gene in Spanish siblings with iodide transport defect

Journal of Clinical Endocrinology and Metabolism

Volumn 87, Issue 8, 2002, Pages 3830-3836

  Kosugi, Shinji ^a   Okamoto, Hiroomi ^a   Tamada, Aiko ^b   Sanchez Franco, F ^a  

^a KYOTO UNIVERSITY   (Japan)

^b HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCINE; IODIDE; METHIONINE; SODIUM;

ARTICLE; CELL MEMBRANE; CELL STRAIN COS7; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; GENE DELETION; GENE MUTATION; GENE SEQUENCE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; INTRON; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SPAIN;

INSERTION SEQUENCES;

EID: 0036348487     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.87.8.8767     Document Type: Article

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21. - symporter in patients with iodide transport defect
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