Today is #RareDiseaseDay – a day to raise awareness for the 300 million people worldwide living with rare diseases. The research carried out at CIBSS uncovers the fundamental mechanisms of cellular function and decision making, helping to explain how disruptions in these processes lead to disease.
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One of them is the Basilicata-Akhtar syndrome, caused by mutations in the MSL3 gene. #CIBSS and @mpi-ie.bsky.social researcher Asifa Akhtar and her team have uncovered how epigenetic dysregulation contributes to this condition https://kurzlinks.de/j9wz
https://kurzlinks.de/ch30