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Article

Mirror syndromes regarding AKT3 mutations: Loss of function variant leading to microcephaly.

American journal of medical genetics. Part A - 1 Nov 2020

Ciaccio Claudia, Cellini Elena, Guerrini Renzo, Pantaleoni Chiara, Masson Riccardo

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 32827175
DOI: 10.1002/ajmg.a.61821

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