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1H magnetic resonance spectroscopy in monocarboxylate transporter 8 gene deficiency.
Paul E PE Sijens, Lars A LA Rödiger, Linda C LC Meiners and Roelineke J RJ Lunsing
J Clin Endocrinol Metab 93(5):1854-9 (2008)
PMID 18319316
In monocarboxylate transporter 8 (MCT8) gene deficiency, a syndrome combining thyroid and neurological abnormalities, the central nervous system has not yet been characterized by magnetic resonance (MR) spectroscopy.
DOI: 10.1210/jc.2007-2441
Version: za2963e q8za7 q8zb8 q8zc3 q8zd5 q8zec q8zf7 q8zga
DOI: 10.1210/jc.2007-2441
Version: za2963e q8za7 q8zb8 q8zc3 q8zd5 q8zec q8zf7 q8zga