Description: Studying new genes mutated in infantile epilepsy and paroxysmal movement disorders to unravel the pathophysiology underlying these diseases. Multi-level approach: genetics, molecular/cellular biology, biochemistry, imaging and proteomics. Different disease models involved: IPSC-derived human models 3D brain organoids knock-out mouse neuronal cultures reproducing gene loss of function mutations.

Employer: Prof.ssa Anna Corradi, PhD.

Location: University of Genova, Department of Experimental Medicine, section of human Phyiology

Duration: One-year renewable position (Assegno di Ricerca)

Application deadline: 20231122

How to apply: Contact Prof.ssa Anna Corradi at the email: acorradi@unige.it

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