CORDIS Project
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This project aims to investigate the genetic basis of rare neurodegenerative diseases using zebrafish models. By studying the effects of specific genetic variants on microtubule dynamics, it seeks to enhance understanding of brain physiology and contribute to the development of therapies.
Circa 30 million people in Europe suffer from life-threatening rare diseases, which are poorly understood.
This major societal burden forces patients into endless paths for a diagnosis often without cure. EU cooperation efforts between countries contribute to improve research and visibility of these diseases with a primary role of the ‘Ospedale pediatrico Bambino Gesù’ (OPBG, Italy).
Here, via next generation sequencing technology, Dr.
Tartaglia recently described new genetic variants, including…
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