Title : Beneficial effects of propylthiouracil plus L-thyroxine treatment in a patient with a mutation in MCT8.

Pub. Date : 2008 Jun

PMID : 18334584






1 Functional Relationships(s)
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Protein Name
Organism
1 Lack of MCT8 transport of T(3) in neurons could explain the neurological phenotype. Triiodothyronine solute carrier family 16 member 2 Homo sapiens