
FAMILY STORY
Family Stories // Historias Familiares: Gabriel (CTNNB1)
Simons Searchlight sat down with the family of Gabriel, who has a genetic change in CTNNB1, to learn about their rare disease journey and their participation in Simons Searchlight. #ShareYourRareStory #ShareYourRare
Simons Searchlight se sentó con la familia de Gabriel, quien tiene un cambio genético en CTNNB1, para aprender sobre su viaje de enfermedades raras y su participación en Simons Searchlight. #Comparteturarahistoria
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