Tissue-specific effects of mutations in the thyroid hormone transporter MCT8
Author:
Affiliation:
1. Erasmus University, The Netherlands
Publisher
FapUNIFESP (SciELO)
Subject
General Medicine,Endocrinology, Diabetes and Metabolism
Link
http://www.scielo.br/pdf/abem/v55n1/01.pdf
Reference20 articles.
1. Cellular and molecular basis of deiodinase-regulated thyroid hormone signaling;Gereben B;Endocr Rev,2008
2. Minireview: thyroid hormone transporters: the knowns and the unknowns;Visser WE;Mol Endocrinol,2011
3. A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene;Dumitrescu AM;Am J Hum Genet,2004
4. Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation;Friesema EC;Lancet,2004
5. Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities;Menezes Filho HC;Arq Bras Endocrinol Metab,2011
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