SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic Features.
Saved in:
| Title: | SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic Features. |
|---|---|
| Authors: | Epifanio R; Clinical Neurophysiology Unit, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, LC, Italy., Giorda R; Molecular Biology Laboratory, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, LC, Italy., Merlano MC; Royal University Hospital, University of Saskatchewan, Saskatoon, SK S7N 0W8, Canada., Zanotta N; Clinical Neurophysiology Unit, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, LC, Italy., Romaniello R; Clinical Neurophysiology Unit, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, LC, Italy., Marelli S; Clinical Neurophysiology Unit, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, LC, Italy., Russo S; Cytogenetics and Molecular Genetics Laboratory, Istituto Auxologico Italiano IRCCS, 20145 Milan, MI, Italy., Cogliati F; Cytogenetics and Molecular Genetics Laboratory, Istituto Auxologico Italiano IRCCS, 20145 Milan, MI, Italy., Bassi MT; Molecular Biology Laboratory, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, LC, Italy., Zucca C; Clinical Neurophysiology Unit, Scientific Institute IRCCS E. Medea, 23842 Bosisio Parini, LC, Italy. |
| Source: | Brain sciences [Brain Sci] 2021 Dec 24; Vol. 12 (1). Date of Electronic Publication: 2021 Dec 24. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: MDPI Country of Publication: Switzerland NLM ID: 101598646 Publication Model: Electronic Cited Medium: Print ISSN: 2076-3425 (Print) Linking ISSN: 20763425 NLM ISO Abbreviation: Brain Sci Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 2076-3425 |
|---|---|
| DOI: | 10.3390/brainsci12010018 |
