Results 1 -
2
of
2
for
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 ...