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Parallel Session: Metabolic and Genetic Diseases

Saturday, November 14
2:00 PM
3:30 PM


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About the Session

Watch this live session to see the top research in Metabolic and Genetic Diseases.  Content will only be aired on this date, at this time. Don't miss it!

  • Death and Long-Term Development of Health Complications in C282Y-Linked Hemochromatosis Patients
    Presenting Author Paul Adams
  • Evaluation of Adenine Base Editing as a Potential Treatment for Alpha-1 Antitrypsin Deficiency
    Presenting Author Michael Packer
  • Treatment of A-1 Antitrypsin Deficiency Using Hepatic-Specified Cells Derived from Human Induced Pluripotent Stem Cells
    Presenting Author Jianqiang Ding
  • Comaprison of Baseline Characteristics and Improvement in Disease Manifestations Following Treatmetn with Sebelipase Alfa in Patients with Lyosomal Acid Deficiency With and Without Cirrhosis
    Presenting Author Rohit Kohli
  • Liver Phenotype of Individuals with Alpha-1 Antitrypsin Deficiency
    Presenting Author Malin Fromme
  • Mitochondrial Dysfunction In Wilson Disease: A Study on Patients and a Mouse Model of Copper Accumulation
    Presenting Author Valentina Medici