Research 2017-08-21T03:09:00+00:00


Cure RTD is dedicated to the treatment and cure of Riboflavin Transporter Deficiency (RTD), a life-threatening, neurodegenerative genetic disorder. We fund groundbreaking research and provide families and physicians the support and guidance they need today.

Research Grant Program

Available funding for basic science and clinical research on the natural history, biochemical basis, and treatment of RTD.   LEARN MORE >   

Cure RTD Registry

Information from individuals with RTD that can be utilized by researchers to better understand RTD.   LEARN MORE >   

Human SLC52 Gene Variants Database

Database of SLC52A2 and SLC52A3 genes found in either homozygous or compound heterozygous state in individuals affected by RTD.  LEARN MORE>   

Scientific & Medical Publications

Cure RTD maintains a vast library of information as it relates to RTD and the various components of this multi-system disorder, which serves both the medical community and affected families.  LEARN MORE>   

For Researchers and Scientists

Information for researchers and scientists carrying out research or interested in RTD. LEARN MORE >