Post published:July 27, 2022 Post category:News Please Share This Share this content Opens in a new window Opens in a new window Opens in a new window Opens in a new window Opens in a new window Opens in a new window Opens in a new window Opens in a new window Opens in a new window Opens in a new window This Post Has One Comment Cody Amerson July 27, 2022 Log in to Reply Thank you for creating and sharing this video. We are excited to see the progress you have made. We have tremendous hope in the work you are doing. This means the world to our family. Thank you. – Cody & Emily Amerson (Savannah’s parents) Leave a Reply Cancel replyYou must be logged in to post a comment. You Might Also Like CTNNB1 Syndrome Included in La Jolla Lab’s ‘Revealing Rare Genes’ Collection June 11, 2024 New Partnership Announcement: REN December 18, 2023 CTNNB1 Connect & Cure Attends Rare Advocate Development Workshop in NYC February 5, 2025
Cody Amerson July 27, 2022 Log in to Reply Thank you for creating and sharing this video. We are excited to see the progress you have made. We have tremendous hope in the work you are doing. This means the world to our family. Thank you. – Cody & Emily Amerson (Savannah’s parents)
Thank you for creating and sharing this video. We are excited to see the progress you have made. We have tremendous hope in the work you are doing. This means the world to our family. Thank you. – Cody & Emily Amerson (Savannah’s parents)