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mct8
- ... Dudley syndrome. The SLC16A2 gene, also known as MCT8, provides instructions for making a protein that plays ... gene mutations in these cases. Allan-Herndon syndrome MCT8 (SLC16A2)-specific thyroid hormone cell transporter deficiency Mental ...
- The SLC16A2 gene (also known as MCT8) provides instructions for making a protein that plays a critical role in nervous system development. This protein transports a particular hormone into ...
- ... Macular Society (UK) Marinesco-Sjogren Syndrome Support Group mct8.org Menkes Foundation Metabolic Support UK MHE Research ...