Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene

American Journal of Human Genetics

Volumn 77, Issue 1, 2005, Pages 41-53

  Schwartz, Charles E ^a   May, Melanie M ^a   Carpenter, Nancy J ^b   Rogers, R Curtis ^a   Martin, Judith ^c   Bialer, Martin G ^d   Ward, Jewell ^e   Sanabria, Javier ^f   Marsa, Silvana ^f   Lewis, James A ^g   Echeverri, Roberto ^a,h   Lubs, Herbert A ^a,h   Voeller, Kytja ^a   Simensen, Richard J ^a   Stevenson, Roger E ^a  

^a GREENWOOD GENETIC CENTER   (United States)

^b Center for Genetic Testing   (United States)

^c Inland NW Genetics Clinic ^*  (United States)

^d University Hospital ^*  (United States)

^e UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^f UNIVERSIDAD NACIONAL DE SAN LUIS   (Argentina)

^g WW Hastings Indian Hospital   (United States)

^h UNIVERSITY OF MIAMI   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; LIOTHYRONINE; MONOCARBOXYLATE TRANSPORTER 8; THYROID HORMONE; THYROXINE; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGGRESSION; ALLAN HERNDON DUDLEY SYNDROME; ARTICLE; ATAXIA; CHROMOSOME MAP; CHROMOSOME XQ; CLINICAL ARTICLE; COGNITIVE DEFECT; COGNITIVE DEVELOPMENT; DISEASE SEVERITY; DYSARTHRIA; FACE MALFORMATION; FAMILIAL DISEASE; FEMALE; GENE; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; GENETIC SCREENING; HIGH RISK POPULATION; HUMAN; MALE; MCT8 GENE; MENTAL RETARDATION MALFORMATION SYNDROME; MOBILIZATION; MUSCLE HYPOTONIA; MUSCLE MASS; MUSCLE WEAKNESS; MYOPATHY; PRIORITY JOURNAL; SPASTICITY; THYROID DISEASE; THYROXINE BLOOD LEVEL; X CHROMOSOME; X LINKED MENTAL RETARDATION;

ATAXIA;

EID: 20544454120     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/431313     Document Type: Article

References (18)

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