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Updated: Dec 11, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Mirror syndromes regarding AKT3 mutations: Loss of function variant leading to microcephaly
Claudia Ciaccio1, Elena Cellini2, Renzo Guerrini2
1Developmental Neurology Department, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
No abstract available in PubMed .
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