ASXL1 Gene Mutation clinical trials at University of California Health

1 research study open to eligible people

Showing trials for

  • ASXL-Related Disorders Registry

    open to all eligible people

    A registry focused on the natural history, management and treatment of patients with Bohring-Opitz Syndrome (ASXL1), Shashi-Pena Syndrome (ASXL2) and Bainbridge-Ropers Syndrome (ASXL3).

    at UCLA

Our lead scientists for ASXL1 Gene Mutation research studies include .

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