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Article

Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 May 2021

Alagia Marianna, Bernardo Pia, Genesio Rita, Gennaro Elena, Brunetti-Pierri Nicola, Coppola Antonietta, Zara Federico, Striano Pasquale, Striano Salvatore, Terrone Gaetano

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PMID: 33201365
DOI: 10.1007/s10072-020-04898-1

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