Information for Researchers

The KAT6A/KAT6B Patient Registry is a centralized source of information on KAT6A and KAT6B syndromes. We encourage researchers to utilize the registry. Interested researchers may apply to:

  1. Access de-identified data.
  2. Notify registry participants about your IRB approved research study.
  3. Add customized questions to the KAT6A/KAT6B Patient Registry.

Researchers interested in requesting support recruiting, access to data, or adding customized questions to the registry should reach out to: kat6a@yahoo.com.

 

“Registries for Rare Diseases: Involve the Patient” http://www.medscape.com/viewarticle/837851?src=par_nord_stm_mscpedt&faf=1 Originally published on Medscape Rare Diseases as part of the NORD and Medscape Editorial Collaboration.