Article
Zebrafish in understanding molecular pathophysiology, disease modeling, and developing effective treatments for Rett syndrome.
The journal of gene medicine - 1 Feb 2024
Pramanik Subrata, Bala Asis, Pradhan Ajay
Abstract excerpt
Rett syndrome (RTT) is a rare but dreadful X-linked genetic disease that mainly affects young girls. It is a neurological disease that affects nerve cell development and function, resulting in severe motor and intellectual disabilities. To date, no cure is available for treating this disease. In 90% of the cases, RTT is caused by a mutation in methyl-CpG-binding protein 2 (MECP2), a transcription factor involved...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
