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Heterozygous nonsense <i>ARX</i> mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co‐inheritanceAlice Traversa, Viviana Caputo, Noemi Panzironi et al.|Molecular Genetics & Genomic Medicine|2020Cited by 4
MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variantsAgnese Giovannetti, Viviana Caputo, Alessandro Bruselles et al.|Human Mutation|2022Cited by 2