DNM1 encephalopathy − atypical phenotype with hypomyelination due to a novel de novo variant in the DNM1 gene. (March 2018)
- Record Type:
- Journal Article
- Title:
- DNM1 encephalopathy − atypical phenotype with hypomyelination due to a novel de novo variant in the DNM1 gene. (March 2018)
- Main Title:
- DNM1 encephalopathy − atypical phenotype with hypomyelination due to a novel de novo variant in the DNM1 gene
- Authors:
- Kolnikova, Miriam
Skopkova, Martina
Ilencikova, Denisa
Foltan, Tomas
Payerova, Jaroslava
Danis, Daniel
Klimes, Iwar
Stanik, Juraj
Gasperikova, Daniela - Abstract:
- Is Part Of:
- Seizure. Volume 56(2018)
- Journal:
- Seizure
- Issue:
- Volume 56(2018)
- Issue Display:
- Volume 56, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 56
- Issue:
- 2018
- Issue Sort Value:
- 2018-0056-2018-0000
- Page Start:
- 31
- Page End:
- 33
- Publication Date:
- 2018-03
- Subjects:
- Dynamin 1 -- DNM1 gene -- Epileptic encephalopathy -- Hypomyelination
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.2018.01.020 ↗
- 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:
- 6323.xml