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A Conversation About Patient Data

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Proudly supported by

Speakers

Hillary Savoie

PhD, Founder/Director TCSF

Gabi Belfort

MD, PhD, Praxis Precision Medicines

John Schreiber

MD, Children's National

Vanessa Vogel-Farley

DUP15Q Alliance and RareX

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Hosted by

The Cute Syndrome Foundation

The Cute Syndrome Foundation raises awareness, funds research, and supports families of people with SCN8A mutations.

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