CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder. (September 2018)
- Record Type:
- Journal Article
- Title:
- CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder. (September 2018)
- Main Title:
- CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder
- Authors:
- Finsterer, Josef
Fiorini, Ana C.
Scorza, Carla A.
Scorza, Fulvio A. - Abstract:
- Is Part Of:
- European journal of paediatric neurology. Volume 22:Number 5(2018:Sep.)
- Journal:
- European journal of paediatric neurology
- Issue:
- Volume 22:Number 5(2018:Sep.)
- Issue Display:
- Volume 22, Issue 5 (2018)
- Year:
- 2018
- Volume:
- 22
- Issue:
- 5
- Issue Sort Value:
- 2018-0022-0005-0000
- Page Start:
- 889
- Page End:
- 891
- Publication Date:
- 2018-09
- Subjects:
- Mitochondrial -- Hereditary neuropathy -- Phenotype -- Genotype -- Multisystem disease -- Lactic acidosis
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.2018.04.012 ↗
- 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:
- 7239.xml