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المؤلفون: Nicita, Francesco, DE LISO, Paola, Danti, FEDERICA RACHELE, Laura, Papetti, Fabiana, Ursitti, Castronovo, Antonella, Allemand, Federico, Elena, Gennaro, Federico, Zara, Pasquale, Striano, Spalice, Alberto, Papetti, Laura
المصدر: Seizure. (1):3-11
مصطلحات موضوعية: Genotype, Monogenic, Clinical Neurology, Biology, medicine.disease_cause, Epileptic encephalopathies, Epilepsy, KCNQ, Genotype-phenotype distinction, Channels, medicine, channels, epilepsy, epileptic encephalopathies, kcnq, monogenic, scn1a, Animals, Humans, SCN1A, Mutation, Brain Diseases, General Medicine, medicine.disease, Neurology, Seizure Disorders, Neuronal Hyperexcitability, Neurology (clinical), Neuroscience
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c524597386bc6d6a9ab72a4c30dd02e