Identification of a structural requirement for thyroid Na+/I- symporter (NIS) function from analysis of a mutation that causes human congenital hypothyroidism

FEBS Letters

Volumn 429, Issue 1, 1998, Pages 36-40

  Levy, Orlie ^a   Ginter, Christopher S ^a   De la Vieja, Antonio ^a   Levy, Daniel ^a   Carrasco, Nancy ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

Congenital hypothyroidism; Iodide; Na+ I symporter; Thyroid; Transport

Indexed keywords

HYDROXYL GROUP; IODIDE; SODIUM ION;

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CONGENITAL HYPOTHYROIDISM; ION TRANSPORT; NONHUMAN; PRIORITY JOURNAL; SITE DIRECTED MUTAGENESIS;

ANIMALS; CARRIER PROTEINS; COS CELLS; HUMANS; HYPOTHYROIDISM; IODINE; ION TRANSPORT; MEMBRANE PROTEINS; MODELS, MOLECULAR; MUTAGENESIS, SITE-DIRECTED; SYMPORTERS;

ANIMALIA;

EID: 0032486458     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(98)00522-5     Document Type: Article

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