58 top medical experts on Aspartylglucosaminuria across 6 countries and 5 U.S. states, including 5 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Aspartylglucosaminuria: A recessively inherited, progressive lysosomal storage disease caused by a deficiency of glycosylasparaginase activity. The lack of this enzyme activity results in the accumulation of N-acetylglucosaminylasparagine (the linkage unit of asparagine-linked glycoproteins) in lysosomes.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Lysosomal Storage Diseases (2,636).
  4. Clinical Trials ClinicalTrials.gov : at least 5 including 1 Completed, 1 Recruiting


  

        

                    


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