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ASXL3 Gene Mutation clinical trials

View clinical trials related to ASXL3 Gene Mutation.

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NCT ID: NCT03303716 Recruiting - ASXL1 Gene Mutation Clinical Trials

ASXL-Related Disorders Registry

Start date: September 20, 2017
Phase:
Study type: Observational [Patient Registry]

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).