Riboflavin-responsive ACAD9 mutation as cause of familial hypertrophic cardiomyopathy. (June 2017)
- Record Type:
- Journal Article
- Title:
- Riboflavin-responsive ACAD9 mutation as cause of familial hypertrophic cardiomyopathy. (June 2017)
- Main Title:
- Riboflavin-responsive ACAD9 mutation as cause of familial hypertrophic cardiomyopathy
- Authors:
- Van Coster, R.
Stepman, H.
Vanlander, A.
Smet, J.
Seneca, S.
Vantroys, E.
De Meirleir, L. - Abstract:
- Is Part Of:
- European journal of paediatric neurology. Volume 21(2017)Supplement 1
- Journal:
- European journal of paediatric neurology
- Issue:
- Volume 21(2017)Supplement 1
- Issue Display:
- Volume 21, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 21
- Issue:
- 1
- Issue Sort Value:
- 2017-0021-0001-0000
- Page Start:
- e137
- Page End:
- Publication Date:
- 2017-06
- Subjects:
- Pediatric neurology -- Periodicals
Nervous System Diseases -- Periodicals
Child -- Periodicals
Infant -- Periodicals
Neurologie pédiatrique -- Périodiques
Pediatric neurology
Electronic journals
Periodicals
Electronic journals
618.928 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10903798 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/10903798 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/10903798 ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1090-3798;screen=info;ECOIP ↗
http://www.elsevier.com/journals ↗
http://www.idealibrary.com/links/toc/ejpn/ ↗
http://www.harcourt-international.com/journals ↗ - DOI:
- 10.1016/j.ejpn.2017.04.1043 ↗
- Languages:
- English
- ISSNs:
- 1090-3798
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.733370
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2864.xml