Skip to content
Donate

CTNNB1 landscape logo
  • 2026 CTNNB1 Conference
  • CTNNB1 Syndrome
    • CTNNB1 and Cerebral Palsy
    • Genetics & Testing
    • CTNNB1 Chat
  • About Us
    • Our Team
    • Scientific Advisory Board
    • Mission and Vision
    • Impact
    • Financials
    • Contact Us
  • Research
    • Publications
    • Research Resources
    • CTNNB1 Grant Program
  • Families
    • Newly Diagnosed
    • Participate in Research
    • Resources
    • Undiagnosed Resources
    • Join the Registry
    • Biorepository Roadshow
  • Get Involved
    • Donate
    • Fundraising
    • Volunteer
  • News & Events
    • Past Conferences
    • Blog
    • Podcast
    • Newsletter
  • Shop
  • Toggle website search
Menu Close

  • 2026 CTNNB1 Conference
  • CTNNB1 Syndrome
    • CTNNB1 and Cerebral Palsy
    • Genetics & Testing
    • CTNNB1 Chat
  • About Us
    • Our Team
    • Scientific Advisory Board
    • Mission and Vision
    • Impact
    • Financials
    • Contact Us
  • Research
    • Publications
    • Research Resources
    • CTNNB1 Grant Program
  • Families
    • Newly Diagnosed
    • Participate in Research
    • Resources
    • Undiagnosed Resources
    • Join the Registry
    • Biorepository Roadshow
  • Get Involved
    • Donate
    • Fundraising
    • Volunteer
  • News & Events
    • Past Conferences
    • Blog
    • Podcast
    • Newsletter
  • Shop

CTNNB1 Syndrome Collaboration with Dr. Jacobs from Tufts University in the news

  • Post published:October 18, 2022
  • Post category:News

https://now.tufts.edu/2022/10/18/tufts-scientist-teams-families-find-treatment-rare-disease#top

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

Leave a Reply Cancel reply

You must be logged in to post a comment.

You Might Also Like

New Research Breakthrough for CTNNB1 Syndrome

February 7, 2025

Dr. Michele Jacob will be speaking at upcoming WNT & B-Catenin Targeted Drug Development Conference about her exciting work to help treat patients with CTNNB1 Syndrome

September 28, 2022
Basket Auction Fundraiser

Basket Auction Fundraiser

May 15, 2023

Blog

  • Dragonflies
  • Educational
  • News
  • Newsletter
  • Research
Donate
  • Opens in a new tab
  • Opens in a new tab
  • Opens in a new tab
  • Opens in a new tab
  • Opens in a new tab
  • Opens in a new tab

221 W 9th St
Ste 421
Wilmington, DE 19801

info@curectnnb1.org

EIN: 83-4541448

The content provided by this website is for educational, communication and information purposes only and is not intended to replace or constitute medical advice or treatments. Consult your own physician.

Privacy Policy

© Copyright 2026 CTNNB1 Connect and Cure, Inc.