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Join Emma Celis, Mito Registry Coordinator, to discuss the benefits of joining the Mitochondrial Disease Patient Registry (Mito Registry). The Mito Registry ensures people impacted by mitochondrial disease (mito) have the earliest possible opportunity to access studies or clinical trials that may result in new treatment options. Limited information is stored on the Mito Registry and is not shared outside of the foundation without your permission.

This Mito Connect Call is a great chance to meet Emma and understand the value of the Mito Registry.

Event Location

Held Online via Zoom.


Thu 11 Mar 2021

Start Time

12:00 pm AEDT

End Time

1:00 pm AEDT

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