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Published in 2021 at "Glia"
DOI: 10.1002/glia.24014
Abstract: Inactivating mutations in the thyroid hormone (TH) transporter monocarboxylate transporter 8 (MCT8) causes a rare and debilitating form of X‐linked psychomotor disability known as Allan Herndon Dudley syndrome (AHDS). One of the most prominent pathophysiological…
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Keywords:
mct8;
across brain;
oligodendrocyte progenitor;
maturation ... See more keywords