Inherited defects in thyroid hormone cell-membrane transport and metabolism

Best Practice and Research: Clinical Endocrinology and Metabolism

Volumn 28, Issue 2, 2014, Pages 189-201

  Fu, Jiao ^a,b   Dumitrescu, Alexandra M ^a  

^a UNIVERSITY OF CHICAGO MEDICAL CENTER   (United States)

^b THE FIRST AFFILIATED HOSPITAL OF XI AN JIAOTONG UNIVERSITY   (China)

Author keywords

Allan Herndon Dudley syndrome; deiodinase; MCT8; SBP2; selenoprotein; thyroid hormone cell membrane transporter

Indexed keywords

LIOTHYRONINE; MONOCARBOXYLATE TRANSPORTER 8; PROTEIN; PROTEIN SBP2; SELENOPROTEIN; THYROXINE; UNCLASSIFIED DRUG;

CELL MEMBRANE TRANSPORT; GENE; GENE MUTATION; HORMONE TRANSPORT; HUMAN; NONHUMAN; REVIEW; SBP2 GENE; THYROID DISEASE; THYROID FUNCTION; THYROID HORMONE METABOLISM;

ALLAN-HERNDON-DUDLEY SYNDROME; DEIODINASE; MCT8; SBP2; SELENOPROTEIN; THYROID HORMONE CELL-MEMBRANE TRANSPORTER;

CELL MEMBRANE; HUMANS; MALE; MEMBRANE TRANSPORT PROTEINS; MENTAL RETARDATION, X-LINKED; MONOCARBOXYLIC ACID TRANSPORTERS; MUSCLE HYPOTONIA; MUSCULAR ATROPHY; RNA-BINDING PROTEINS; SELENOPROTEINS; THYROTROPIN; THYROXINE; TRIIODOTHYRONINE; TRIIODOTHYRONINE, REVERSE;

EID: 84896089325     PISSN: 1521690X     EISSN: 15321908     Source Type: Journal    
DOI: 10.1016/j.beem.2013.05.014     Document Type: Review

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