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News

Posted on 10/17/2024

The peer-reviewed paper, "A Roadmap to Cure CHD2-Related Disorders," by CCC's board and Scientific Advisory Board has been published in the journal, Therapeutic Advances in Rare Disease.

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Posted on 11/08/2024

Board Co-President Brian Broadbent has worked tirelessly to find treatment for his daughter Emma, who has a change in the CHASERR gene, which causes her to have too much, instead of too little, CHD2, with profound impact. A study of Emma was recently published.

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