Myoclonic epilepsy of infancy related to YWHAG gene mutation: towards a better phenotypic characterization. (January 2022)
- Record Type:
- Journal Article
- Title:
- Myoclonic epilepsy of infancy related to YWHAG gene mutation: towards a better phenotypic characterization. (January 2022)
- Main Title:
- Myoclonic epilepsy of infancy related to YWHAG gene mutation: towards a better phenotypic characterization.
- Authors:
- Iodice, Alessandro
Giannelli, Costanza
Soli, Fiorenza
Riva, Antonella
Striano, Pasquale - Abstract:
- Is Part Of:
- Seizure. Volume 94(2022)
- Journal:
- Seizure
- Issue:
- Volume 94(2022)
- Issue Display:
- Volume 94, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 94
- Issue:
- 2022
- Issue Sort Value:
- 2022-0094-2022-0000
- Page Start:
- 161
- Page End:
- 164
- Publication Date:
- 2022-01
- Subjects:
- Myoclonic Epilepsy -- YWHAG -- Gene developmental and epileptic enchephalopathy -- Neurodevelopmental disorders
Epilepsy -- Periodicals
Epilepsy -- Periodicals
Seizures -- Periodicals
Épilepsie -- Périodiques
Electronic journals
Electronic journals
616.853 - Journal URLs:
- http://www.seizure-journal.com/ ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/13550306 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/10591311 ↗
http://www.sciencedirect.com/science/journal/10591311 ↗
http://www.elsevier.com/journals ↗
http://www.harcourt-international.com/journals/seiz/ ↗ - DOI:
- 10.1016/j.seizure.2021.12.002 ↗
- Languages:
- English
- ISSNs:
- 1059-1311
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8229.100000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20294.xml