Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8
Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8
About this item
Full title
Author / Creator
Publisher
United States: American Society for Clinical Investigation
Journal title
Language
English
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Publisher
United States: American Society for Clinical Investigation
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Scope and Contents
Contents
In humans, inactivating mutations in the gene of the thyroid hormone transporter monocarboxylate transporter 8 (MCT8; SLC16A2) lead to severe forms of psychomotor retardation combined with imbalanced thyroid hormone serum levels. The MCT8-null mice described here, however, developed without overt deficits but also exhibited distorted 3,5,3'-triiodo...
Alternative Titles
Full title
Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1797602
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1797602
Other Identifiers
ISSN
0021-9738
E-ISSN
1558-8238
DOI
10.1172/jci28253
