Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism

Journal of Clinical Endocrinology and Metabolism

Volumn 93, Issue 12, 2008, Pages 4894-4901

  Afink, Gijs ^a   Kulik, Willem ^a   Overmars, Henk ^a   De Randamie, Janine ^a   Veenboer, Truus ^a   Van Cruchten, Arno ^a   Craen, Margarita ^b   Ris Stalpers, Carrie ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b GHENT UNIVERSITY HOSPITAL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

3,5 DIODOTYROSINE; IODIDE PEROXIDASE; IODOTYROSINE; IODOTYROSINE DEHALOGENASE; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CASE REPORT; CONSANGUINEOUS MARRIAGE; CONTROLLED STUDY; CULTURE MEDIUM; ENZYME ACTIVITY; EXON; GENE MUTATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN CELL; HYPOTHYROIDISM; MASS SPECTROMETRY; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; URINE;

EID: 57349097244     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2008-0865     Document Type: Article

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