Article
Integrated CHARGE syndrome models reveal epigenetic modulators of reproductive phenotypes
2026-04-02
Abstract excerpt
Loss-of-function variants in CHD7 cause CHARGE syndrome (CS), a rare developmental disorder showing multisystem malformations, including reproductive defects linked to gonadotropin-releasing hormone (GnRH) neuron dysfunction. CHD7 encodes a chromatin remodeler essential for early transcriptional regulation across various tissues. Currently, no pharmacological treatments exist, and approaches aimed at identifying...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- a2dec7fc-287b-5757-9cf9-fbfdf5e1ae0e
- DOI
- 10.64898/2026.03.31.715488
