Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8

Endocrinology

Volumn 149, Issue 5, 2008, Pages 2184-2190

  Jansen, Jurgen ^a   Friesema, Edith C H ^a   Kester, Monique H A ^a   Schwartz, Charles E ^b   Visser, Theo J ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b GREENWOOD GENETIC CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; LIOTHYRONINE; MONOCARBOXYLATE TRANSPORTER 8; THYROXINE;

ANIMAL CELL; ARTICLE; CELL STRAIN COS1; CONTROLLED STUDY; GENE MUTATION; GENETIC TRANSFECTION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HUMAN CELL; IMMUNOCYTOCHEMISTRY; LIOTHYRONINE METABOLISM; MAJOR CLINICAL STUDY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PSYCHOMOTOR DEVELOPMENT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; THYROXINE METABOLISM; WESTERN BLOTTING;

ANIMALS; CELLS, CULTURED; CERCOPITHECUS AETHIOPS; COS CELLS; CRYSTALLINS; GENOTYPE; HUMANS; MONOCARBOXYLIC ACID TRANSPORTERS; MUTAGENESIS, SITE-DIRECTED; MUTATION; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PSYCHOMOTOR PERFORMANCE; THYROID HORMONES; TRANSFECTION;

EID: 42449161045     PISSN: 00137227     EISSN: 00137227     Source Type: Journal    
DOI: 10.1210/en.2007-1475     Document Type: Article

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