Regina Proskorovski-Ohayon
2PUBLICATIONS
20CO-AUTHORS
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Publications (2)
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|Jan 25, 2023
Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation.Amit Safran, Regina Proskorovski-Ohayon, Marina Eskin-Schwartz
|Oct 27, 2021
CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice.D Halperin, A Stavsky, R Kadir
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