90 top medical experts on Deficiency of Member 9 Acyl-CoA Dehydrogenase Family across 12 countries and 2 U.S. states, including 6 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Deficiency of Member 9 Acyl-CoA Dehydrogenase Family: A rare disorder characterized by neurological dysfunction, hepatic failure and cardiomyopathy due to a deficiency of complex I of the respiratory chain.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:


  

        

                    


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