Thyroid hormone transporter defects

Endocrine Development

Volumn 10, Issue , 2007, Pages 118-126

  Gruters A ^a,b  

^a FREIE UNIVERSITÄT BERLIN   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MONOCARBOXYLATE TRANSPORTER; SLC16A2 PROTEIN, HUMAN; THYROID HORMONE; UNCLASSIFIED DRUG;

ANIMAL; GENE DELETION; GENETICS; HUMAN; METABOLISM; MOUSE; MOUSE MUTANT; MUTATION; NERVE CELL; NEUROLOGIC DISEASE; PHENOTYPE; PHYSIOLOGY; REVIEW; THYROID DISEASE; X CHROMOSOME;

ANIMALS; CHROMOSOMES, HUMAN, X; GENE DELETION; HUMANS; MICE; MICE, KNOCKOUT; MONOCARBOXYLIC ACID TRANSPORTERS; MUTATION; NERVOUS SYSTEM DISEASES; NEURONS; PHENOTYPE; THYROID DISEASES; THYROID HORMONES;

EID: 35148880836     PISSN: 14217082     EISSN: 16622979     Source Type: Book Series    
DOI: 10.1159/000106823     Document Type: Review

References (17)

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