MCT8 Research Project
Project Member(s): Milthorpe, B.
Funding or Partner Organisation: The Trustee for Sherman Foundation
Start year: 2014
Summary: This project undertakes and coordinates research into the characterisation, causes and treatments for a rare genetic disease of the thyroid hormone transporting protein MCT8.
Keywords: monocarboxylase transporter 8, genetic diseases, rare diseases
FOR Codes: Nervous System and Disorders, Care for Disabled, Inherited Diseases (incl. Gene Therapy), Biochemistry and Cell Biology, Neurosciences, People with disability, Clinical health