Patients with CTNNB1 Syndrome will benefit from this joint effort to develop and manufacture a new AAV investigational gene therapy, which aims to restore gene function and may improve quality of life ...
Add Yahoo as a preferred source to see more of our stories on Google. GARRETSON, S.D. (KELO) — July 25 is the awareness day for a very rare syndrome, but one that a local child has. Carter Dreckman is ...
Loss-of-function mutations in the CTNNB1 gene cause β-catenin deficiency, leading to CTNNB1 syndrome, a rare neurodevelopmental disorder marked by motor and cognitive impairments. Because the disease ...
A south metro family is getting closer to their 2-year-old possibly joining a first-of-its-kind gene therapy as the community rallies around them to fundraise. We first told you about Lucy Hieb in ...
MOBILE, Ala. (WALA) - Shreve McWilliams is so happy every day despite the challenges that she has faced since she was born. Her parents discovered through private genetic testing that she has a very ...
Henry’s Club of Algonac is gearing up to host PJ 5K for JP, a 5K run that will take place Dec. 14 to benefit the journey of local toddler Jack Parker, called JP, who has CTNNB1 syndrome, as well as ...
David joined the WCCO team in April 2020, previously working at CBS 58 in Milwaukee. Prior to that, he worked in Las Vegas. While there, David covered several stories in the national spotlight, ...
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