Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
Other Names for this Disease
- CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F
- GNB4-related intermediate Charcot-Marie-Tooth neuropathy
- The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.
- The Inherited Neuropathies Consortium is a team of doctors, nurses, research coordinators, and research labs throughout the U.S., working together to improve the lives of people with Charcot Marie Tooth disease through research. The Inherited Neuropathies Consortium has a registry for patients who wish to be contacted about clinical research opportunities.
For more information on the registry see: http://rarediseasesnetwork.epi.usf.edu/INC/register/index.htm