Structural analysis and genetic code expansion reveal the functional impact of NR2F1 mutations associated with BBSOA-Syndrome biorxiv.org/content/10.110…

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Pathophysiological Mechanism of Neurodevelopmental Disorders mdpi.com/si/83523 #mdpicells via MDPI

A postdoctoral position is available in my lab from January/February 2021 to understand the pathological contribution of single NR2F1 variants in the mouse system, and in patient-derived human organoids.

Thank you to all for your kind welcome! Hope you are all well😀 Difficult times...but we have to go ahead!