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Publications by Nicoletta Zanotta

Novel Epilepsy Phenotype Associated to a Known SCN8A Mutation

Seizure : the journal of the British Epilepsy Association

English

Long-Term Follow-Up of a Patient With 5q31.3 Microdeletion Syndrome and the Smallest De Novo 5q31.2q31.3 Deletion Involving PURA

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

English